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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items trans-2-Chloromethylvinylboronic acid (contains varying amounts of Anhydride) - ≥95% Cat. No.: I168619
Synonyms
AKOS015848709 | C3H6BClO2 | (3-Chloroprop-1-en-1-yl)boronic acid | MFCD01074546 | (E)-3-chloroprop-1-enylboronic acid | BS-22511 | J-014166 | AMY1186 | NCGC00249449-01 | B-[(1E)-3-Chloro-1-propen-1-yl]boronic acid | (E)-(3-chloroprop-1-en-1-yl)boronic aci
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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.
Descripción general Reactant for Suzuki-Miyaura cross-coupling reaction.
Specifications Sinónimos
AKOS015848709 | C3H6BClO2 | (3-Chloroprop-1-en-1-yl)boronic acid | MFCD01074546 | (E)-3-chloroprop-1-enylboronic acid | BS-22511 | J-014166 | AMY1186 | NCGC00249449-01 | B-[(1E)-3-Chloro-1-propen-1-yl]boronic acid | (E)-(3-chloroprop-1-en-1-yl)boronic aci
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 488195648 Sonrisas canónicas B(C=CCCl)(O)O IUPAC Name [(E)-3-chloroprop-1-enyl]boronic acid InChIKey JMTGSXGIIONQHI-OWOJBTEDSA-N INCHI 1S/C3H6BClO2/c5-3-1-2-4(6)7/h1-2,6-7H,3H2/b2-1+
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 Organic acids and derivatives Clase Boronic acid derivatives Subclass Boronic acids Intermediate Tree Nodes Not available Direct Parent Boronic acids Alternative Parents Organic metalloid salts Organometalloid compounds Organochlorides Organic oxygen compounds Hydrocarbon derivatives Alkyl chlorides Molecular Framework Aliphatic acyclic compounds Substituents Boronic acid - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organochloride - Organic metalloid moeity - Organohalogen compound - Alkyl halide - Alkyl chloride - Aliphatic acyclic compound Descripción This compound belongs to the class of organic compounds known as boronic acids. These are compounds comprising the boronic acid functional group RB(O)O (R,R'=alkyl, aryl). 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 120.340 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 2 Exact Mass 120.015 Da Monoisotopic Mass 120.015 Da Topological Polar Surface Area 40.500 Ų Heavy Atom Count 7 Formal Charge 0 Complexity 64.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 1
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