4-Phenoxyphenylboronic Acid (contains varying amounts of Anhydride) - ≥96% , CAS No.51067-38-0

CAS: 51067-38-0 Cat. No.: P102933 Molecular Weight: 214.02 EC Number: 687-755-5
AVAILABLE TO ORDER
GRADE & PURITY ≥96%
Synonyms
4-Phenoxybenzeneboronic acid | A828424 | SCHEMBL9285 | HY-76584 | MFCD00093312 | AMY479 | BCP27808 | SY014269 | J-515926 | P1974 | GS-6829 | (4-Phenoxyphenyl)boronic acid;4-Phenoxyphenylboronic acid | FT-0619375 | KFXUHRXGLWUOJT-UHFFFAOYSA-N | Z381541034
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
P102933-1g
4
$9.90
5g
P102933-5g
5
$10.90
10g
P102933-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$14.90

$22.90
Save $8.00 (34.93%)
25g
P102933-25g
4

$24.90

$37.90
Save $13.00 (34.30%)
100g
P102933-100g
2

$71.90

$107.90
Save $36.00 (33.36%)
500g
P102933-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$358.90

$538.90
Save $180.00 (33.40%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
4-Phenoxybenzeneboronic acid | A828424 | SCHEMBL9285 | HY-76584 | MFCD00093312 | AMY479 | BCP27808 | SY014269 | J-515926 | P1974 | GS-6829 | (4-Phenoxyphenyl)boronic acid;4-Phenoxyphenylboronic acid | FT-0619375 | KFXUHRXGLWUOJT-UHFFFAOYSA-N | Z381541034
Specifications & Purity
≥96%
Storage
Room temperature
Shipped In
Normal
Purity
≥96%
Names and Identifiers
Pubchem Sid488192563
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488192563
Canonical SmilesB(C1=CC=C(C=C1)OC2=CC=CC=C2)(O)O
IUPAC Name(4-phenoxyphenyl)boronic acid
InChIKeyKFXUHRXGLWUOJT-UHFFFAOYSA-N
INCHI1S/C12H11BO3/c14-13(15)10-6-8-12(9-7-10)16-11-4-2-1-3-5-11/h1-9,14-15H
Isomeric SMILES B(C1=CC=C(C=C1)OC2=CC=CC=C2)(O)O
WGK Germany 3
Molecular Weight 214.02
Reaxy-Rn 2846397
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2846397&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
SubclassDiphenylethers
Intermediate Tree Nodes Not available
Direct ParentDiphenylethers
Alternative Parents Diarylethers  Phenoxy compounds  Phenol ethers  Boronic acids  Organic metalloid salts  Organoboron compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Diphenylether - Diaryl ether - Phenoxy compound - Phenol ether - Boronic acid - Boronic acid derivative - Organic metalloid salt - Ether - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organoboron compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Faah Anandamide amidohydrolase (3907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dac D-alanyl-D-alanine carboxypeptidase (132 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.

13 results found

Lot NumberCertificate TypeDateItem
L2121026Certificate of AnalysisOct 11, 2025 P102933
J2513519Certificate of AnalysisJul 12, 2024 P102933
J2513533Certificate of AnalysisJul 12, 2024 P102933
J2513536Certificate of AnalysisJul 12, 2024 P102933
J2522751Certificate of AnalysisJul 12, 2024 P102933
K1926147Certificate of AnalysisSep 08, 2023 P102933
D2324677Certificate of AnalysisJun 21, 2022 P102933
J2229257Certificate of AnalysisJun 21, 2022 P102933
J2229292Certificate of AnalysisJun 21, 2022 P102933
J2229324Certificate of AnalysisJun 21, 2022 P102933
J2229385Certificate of AnalysisJun 21, 2022 P102933
J2229391Certificate of AnalysisJun 21, 2022 P102933
C2209248Certificate of AnalysisMar 23, 2022 P102933

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Chemical and Physical Properties
SolubilitySoluble in Methanol
Melt Point(°C)141-145°C
Molecular Weight214.030 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass214.08 Da
Monoisotopic Mass214.08 Da
Topological Polar Surface Area49.700 Ų
Heavy Atom Count16
Formal Charge0
Complexity196.000
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. Shiyan Yue, Xiaoming Ye, Tiegui Nan, Chen Li, Luqi Huang, Yuan Yuan.  (2025)  Daidzin from Pueraria thomsonii regulate root plasticity and cell proliferation.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2025.121228]
Solution Calculators
Reviews

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