Formylphenylboronic acid (contains varying amounts of Anhydride) - ≥98% , CAS No.40138-16-7

CAS: 40138-16-7 Cat. No.: F103251 Molecular Weight: 149.94 Beilstein Registry Number: 3030776 EC Number: 628-526-1
AVAILABLE TO ORDER
GRADE & PURITY ≥98%
Synonyms
2-Boronobenzaldehyde(contains varying amounts of Anhydride) | 2-Formylbenzeneboronic acid(contains varying amounts of Anhydride) | o-Formylbenzeneboronic acid(contains varying amounts of Anhydride) | o-Formylphenylboronic acid(contains varying amounts of
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
F103251-1g
3
$9.90
5g
F103251-5g
5
$10.90
10g
F103251-10g
2
$15.90
25g
F103251-25g
3

$21.90

$39.90
Save $18.00 (45.11%)
100g
F103251-100g
1

$79.90

$129.90
Save $50.00 (38.49%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
2-Boronobenzaldehyde(contains varying amounts of Anhydride) | 2-Formylbenzeneboronic acid(contains varying amounts of Anhydride) | o-Formylbenzeneboronic acid(contains varying amounts of Anhydride) | o-Formylphenylboronic acid(contains varying amounts of
Specifications & Purity
≥98%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%
Names and Identifiers
Pubchem Sid504758345
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758345
Canonical SmilesB(C1=CC=CC=C1C=O)(O)O
IUPAC Name(2-formylphenyl)boronic acid
InChIKeyDGUWACLYDSWXRZ-UHFFFAOYSA-N
INCHI1S/C7H7BO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5,10-11H
Isomeric SMILES B(C1=CC=CC=C1C=O)(O)O
WGK Germany 3
Molecular Weight 149.94
Beilstein 3030776
Reaxy-Rn 3030776
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3030776&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzoyl derivatives
Intermediate Tree Nodes Not available
Direct ParentBenzoyl derivatives
Alternative Parents Benzaldehydes  Boronic acids  Organic metalloid salts  Organoboron compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzoyl - Benzaldehyde - Aryl-aldehyde - Boronic acid - Boronic acid derivative - Organic metalloid salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organoboron compound - Aldehyde - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ACHN (49357 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAKI-1 (44928 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCRF-CEM (65223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
COLO 205 (50209 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DU-145 (51482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KM12 (47707 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
M14 (47487 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MOLT-4 (49676 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-3 (48710 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-4 (44535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-5 (45555 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-8 (47708 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPMI-8226 (44974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXF 393 (41971 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-295 (48000 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-2 (46422 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-28 (48833 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-OV-3 (52876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SN12C (47755 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNB-19 (46794 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TK-10 (45540 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-251 (51189 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-257 (46019 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-62 (47335 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UO-31 (46270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
786-0 (47912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI/ADR-RES (33767 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
T47D (39041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EKVX (44102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H322M (45589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hs-578T (29457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-268 (49410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IGROV-1 (47897 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LOX IMVI (44321 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HOP-62 (47048 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-435 (38290 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNB-75 (44215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H226 (44470 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H522 (44358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BT-549 (31254 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-539 (44845 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

21 results found

Lot NumberCertificate TypeDateItem
G2222463Certificate of AnalysisMay 09, 2026 F103251
G2222442Certificate of AnalysisMay 09, 2026 F103251
A2605385Certificate of AnalysisDec 22, 2025 F103251
A2605386Certificate of AnalysisDec 22, 2025 F103251
A2606591Certificate of AnalysisDec 22, 2025 F103251
A2605384Certificate of AnalysisDec 22, 2025 F103251
G2117089Certificate of AnalysisMay 09, 2025 F103251
G2117088Certificate of AnalysisMay 09, 2025 F103251
L2503048Certificate of AnalysisJun 15, 2024 F103251
K2507104Certificate of AnalysisJun 15, 2024 F103251
F2428186Certificate of AnalysisJun 15, 2024 F103251
F2428185Certificate of AnalysisJun 15, 2024 F103251
F2428184Certificate of AnalysisJun 15, 2024 F103251
F2428183Certificate of AnalysisJun 15, 2024 F103251
F2428182Certificate of AnalysisJun 15, 2024 F103251
C2521437Certificate of AnalysisApr 13, 2024 F103251
I1923070Certificate of AnalysisJul 10, 2023 F103251
E1923039Certificate of AnalysisMar 09, 2023 F103251
F2325071Certificate of AnalysisJul 03, 2022 F103251
G2222461Certificate of AnalysisJul 03, 2022 F103251
F2301029Certificate of AnalysisJul 03, 2022 F103251

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Chemical and Physical Properties
SolubilitySoluble in Methanol
SensitivityMoisture sensitive
Melt Point(°C)115-120°C
Molecular Weight149.940 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass150.049 Da
Monoisotopic Mass150.049 Da
Topological Polar Surface Area57.500 Ų
Heavy Atom Count11
Formal Charge0
Complexity138.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Liu Xun, Si Wenting, Zhao Ziyin, Liu Ningyu, Yang Qiang, Zhou Renxiang, Zhu Rongying, Duan Shanzhou, Chen Yongbing, Yin Lichen.  (2023)  Engineering blood-brain barrier-permeable and tumor cell-ingestible pro-proteins for glioblastoma treatment.  Science China-Chemistry,      [PMID:] [10.1007/s11426-023-1684-5]
2. Feixue Sun, Qi Yao, Yiting Wang, Jiemin Lou, Qiang Li, Qian Tao, Guiying Li.  (2023)  Self-healing injectable stimuli responsive polysaccharide hydrogel constructed with dynamic covalent bonds.  JOURNAL OF APPLIED POLYMER SCIENCE,  140  (34): (e54304).  [PMID:] [10.1002/app.54304]
3. Hongzhi Zhao, Bin Chen, Xiaoyue Zhang, Yan Xiong, Ming Duan.  (2022)  Preparation of Copolymer of Dihydroxy Monomer and Acrylamide and Its Solution Properties with Polyphenylboronic Acid Compounds.  ChemistrySelect,  (39): (e202203264).  [PMID:] [10.1002/slct.202203264]
4. Junjie Deng, Weide Xu, Siyun Lei, Wanyu Li, Qinghua Li, Kaiqiang Li, Jianxin Lyu, Jilong Wang, Zhen Wang.  (2022)  Activated Natural Killer Cells-Dependent Dendritic Cells Recruitment and Maturation by Responsive Nanogels for Targeting Pancreatic Cancer Immunotherapy.  Small,  18  (44): (2203114).  [PMID:36148846] [10.1002/smll.202203114]
5. Wei Liu, Xiaoge Wang, Danyang Zhou, Xiangze Fan, Jinhua Zhu, Xiuhua Liu.  (2022)  A Dioscorea opposita Thunb Polysaccharide-Based Dual-Responsive Hydrogel for Insulin Controlled Release.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  23  (16): (9081).  [PMID:36012342] [10.3390/ijms23169081]
6. Wei Liu, Jianping Ding, Yukun Chen.  (2022)  Thermoplastic vulcanizates dynamically cross-linked by a tailored small molecule.  POLYMERS FOR ADVANCED TECHNOLOGIES,  33  (10): (3418-3429).  [PMID:] [10.1002/pat.5793]
7. Qiao Luo, Nianlan Cheng, Yongqing Yang, Ni Shao, Tianqi Nie, Jifeng Chen, Cuiqing Huang, Siqi Zhang, Yanyu Huang, Chon Man Ieong, Xiaokai Zhang, Kuan Hu, Zeyu Xiao, Liangping Luo.  (2025)  Multi-stage cooperative ROS-responsive hydrogel platform for drug delivery in myocardial ischemia-reperfusion injury repair.  Materials Today Bio,      [PMID:40487180] [10.1016/j.mtbio.2025.101854]
8. Ruping Li, Yanxin Wu, Lvchen He, Ruotong Yang, Kaipei Luo, Fei Gao, Haipo Yuan, Yu Zheng, Yao He.  (2025)  Chinese herb-crosslinked polysaccharide hydrogel loading DFO accelerates diabetes wound healing.  MATERIALS & DESIGN,      [PMID:] [10.1016/j.matdes.2025.114128]
9. Yinxia Dong, LiBo Tong, Xiangjun Li, Miaomiao Li, Wenting Liu, Rongtao Wu, Xinyu Wang, Shiwei Xu, Kuai-She Wang.  (2026)  Photosynthesis-Inspired Dual-Mode Self-Healing Coatings: Leveraging Peony-like ZnO for Corrosion Interception and Energy Harvesting.  Journal of Materials Chemistry A,      [PMID:] [10.1039/D5TA07598J]
10. Manxuan Liu, Zhongcheng Li, Qian Ren, Ziqian Lu, Yubing Zhang, Yili Guo, Ruomeng Li, Die Hu, Linglin Zhang.  (2026)  A Glucose-Responsive Intelligent Antibacterial and Oxygen-Producing Hydrogel Promotes the Healing of Diabetic Wounds by Regulating Cellular Heterogeneity.  Advanced Science,      [PMID:41619261] [10.1002/advs.202517028]
11. Jiao Yuchen, Zhou Ming, Pu Bo, Yang Xiaoling, Li Chenyiting, Xia Liangliang, Deng Guilin, Wei Yunyao, Zhong Jing, Wu Zheng, Chen Shi, Wang Jian, Zhou Yujun.  (2026)  Preparation of room-temperature self-healing recyclable polyurethane elastomers based on a multiple hydrogen/nitrogen coordination boro-oxygen bonds system.  JOURNAL OF POLYMER RESEARCH,  33  (3): (114).  [PMID:] [10.1007/s10965-025-04746-w]
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