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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 5-Bromo-2,3-dihydrobenzo[b]furan-7-boronic acid - ≥95% , CAS No.690632-72-5
Synonyms
DTXSID80383429 | 5-Bromo-2,3-dihydrobenzo[b]furan-7-boronic Acid | SCHEMBL616067 | AKOS015835862 | BS-24751 | MFCD06200893 | (5-bromo-2,3-dihydro-1-benzofuran-7-yl)boronic acid | 5-Bromo-2,3-dihydrobenzo[b]furane-7-boronic acid | 5-bromo-2,3-dihydrobenzof
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Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
DTXSID80383429 | 5-Bromo-2, 3-dihydrobenzo[b]furan-7-boronic Acid | SCHEMBL616067 | AKOS015835862 | BS-24751 | MFCD06200893 | (5-bromo-2, 3-dihydro-1-benzofuran-7-yl)boronic acid | 5-Bromo-2, 3-dihydrobenzo[b]furane-7-boronic acid | 5-bromo-2, 3-dihydrobenzof
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Sonrisas canónicas B(C1=CC(=CC2=C1OCC2)Br)(O)O IUPAC Name (5-bromo-2,3-dihydro-1-benzofuran-7-yl)boronic acid InChIKey BSSWVOKZPQTKGW-UHFFFAOYSA-N INCHI 1S/C8H8BBrO3/c10-6-3-5-1-2-13-8(5)7(4-6)9(11)12/h3-4,11-12H,1-2H2 Isómeros SMILES B(C1=CC(=CC2=C1OCC2)Br)(O)O Peso molecular 242.9 Reaxy-Rn 15432646 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=15432646&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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Clase Coumarans Subclass Not available Intermediate Tree Nodes Not available Direct Parent Coumarans Alternative Parents Alkyl aryl ethers Benzenoids Aryl bromides Boronic acids Oxacyclic compounds Organic metalloid salts Organobromides Organoboron compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Coumaran - Alkyl aryl ether - Aryl bromide - Aryl halide - Benzenoid - Boronic acid derivative - Boronic acid - Oxacycle - Organic metalloid salt - Ether - Organohalogen compound - Hydrocarbon derivative - Organic salt - Organic oxygen compound - Organoboron compound - Organobromide - Organooxygen compound - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as coumarans. These are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Peso molecular 242.860 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 1 Exact Mass 241.975 Da Monoisotopic Mass 241.975 Da Topological Polar Surface Area 49.700 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 190.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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