Ácido benzofurano-2-borónico (contiene cantidades variables de anhídrido) - ≥98% , CAS No.98437-24-2

CAS: 98437-24-2 Cat. No.: B120550 Peso molecular: 161.95 Beilstein Registry Number: 1637889 Número EC: 671-849-8
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
2-benzo[b]furanboronic acid | 2-benzofuraneboronic acid | AS-2627 | Phenylboronic acid, 21 | B2978 | SCHEMBL147973 | benzo[b]furan-2-boronicacid | 2-Benzofuranboronic acid | 2-benzofuran-boronic acid | 2-BENZOFURANYLBORONIC ACID | Z1255383399 | NCGC000920
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
B120550-1g
3

12,90US$

19,90US$
Guardar 7,00 US$ (35.18%)
5g
B120550-5g
3

22,90US$

34,90US$
Guardar 12,00 US$ (34.38%)
10g
B120550-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

34,90US$

52,90US$
Guardar 18,00 US$ (34.03%)
25g
B120550-25g
2

81,90US$

122,90US$
Guardar 41,00 US$ (33.36%)
100g
B120550-100g
1

323,90US$

485,90US$
Guardar 162,00 US$ (33.34%)
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🧪

Why this grade

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

🌡

Storage & shipping

Argon charged,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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
2-benzo[b]furanboronic acid | 2-benzofuraneboronic acid | AS-2627 | Phenylboronic acid, 21 | B2978 | SCHEMBL147973 | benzo[b]furan-2-boronicacid | 2-Benzofuranboronic acid | 2-benzofuran-boronic acid | 2-BENZOFURANYLBORONIC ACID | Z1255383399 | NCGC000920
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504761936
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504761936
Sonrisas canónicasB(C1=CC2=CC=CC=C2O1)(O)O
IUPAC Name1-benzofuran-2-ylboronic acid
InChIKeyPKRRNTJIHGOMRC-UHFFFAOYSA-N
INCHI1S/C8H7BO3/c10-9(11)8-5-6-3-1-2-4-7(6)12-8/h1-5,10-11H
Isómeros SMILES B(C1=CC2=CC=CC=C2O1)(O)O
WGK Alemania 3
Peso molecular 161.95
Beilstein 1637889
Reaxy-Rn 1637889
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1637889&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
SuperclassOrganoheterocyclic compounds
ClaseBenzofurans
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentBenzofurans
Alternative Parents Benzenoids  Heteroaromatic compounds  Furans  Boronic acids  Oxacyclic compounds  Organic metalloid salts  Organooxygen compounds  Organoboron compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Benzofuran - Benzenoid - Heteroaromatic compound - Furan - Boronic acid - Boronic acid derivative - Oxacycle - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Organoboron compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PRSS2 Tchem Trypsin II (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGER3 Tclin Prostanoid EP3 receptor (1985 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MGLL Tchem Monoglyceride lipase (1909 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
ampC Beta-lactamase AmpC (62480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Alpha-chymotrypsin (819 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Faah Anandamide amidohydrolase (3907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

6 results found

Lot NumberCertificate TypeFechaArticulo
C2218086Certificate of AnalysisJan 19, 2026 B120550
C2218087Certificate of AnalysisJan 19, 2026 B120550
C2218088Certificate of AnalysisJan 19, 2026 B120550
C2218090Certificate of AnalysisJan 19, 2026 B120550
I2109138Certificate of AnalysisJun 11, 2025 B120550
C1714110Certificate of AnalysisNov 05, 2024 B120550
Propiedades químicas y físicas
SolubilidadSoluble in water.
SensibilidadMoisture sensitive.
Punto de inflamación (°C)159.7ºC
Punto de ebullición (°C)340.4ºC
Punto de fusión (°C)114-116°C
Peso molecular161.950 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass162.049 Da
Monoisotopic Mass162.049 Da
Topological Polar Surface Area53.600 Ų
Heavy Atom Count12
Formal Charge0
Complexity162.000
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
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Fan Wang, Weiqi Wang, Yuqing Wang, Lili Zhang, Yoshio Okamoto, Jun Shen.  (2023)  Cellulose/amylose derivatives bearing bulky substituents as reversible fluorescent sensors for detection of Fe3+.  CARBOHYDRATE POLYMERS,      [PMID:37659827] [10.1016/j.carbpol.2023.121249]
2. Fan Wang, Weiqi Wang, Yuqing Wang, Wei Zheng, Ting Zheng, Lili Zhang, Yoshio Okamoto, Jun Shen.  (2023)  Synthesis of amylose and cellulose derivatives bearing bulky pendants for high-efficient chiral fluorescent sensing.  CARBOHYDRATE POLYMERS,      [PMID:37028880] [10.1016/j.carbpol.2023.120769]
Calculadoras de soluciones
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