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· · COA & SDS available for every product · Same-day shipping on in-stock items Cyclohexene-1-boronic acid (Contains varying amounts of acid content) - ≥97% , CAS No.89490-05-1
Synonyms
cyclohexene boronic acid | FT-0600679 | AC-31779 | XZWQKJXJNKYMAP-UHFFFAOYSA-N | cyclohex-1-en-1-ylboronicacid | cyclohex-1-en-1-yl boronic acid | cyclohexenylboronic acid | SCHEMBL150150 | CYCLOHEX-1-ENYLBORONIC ACID | cyclohex-1-en-ylboronic acid
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Why this grade ≥97% 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 Synonyms
cyclohexene boronic acid | FT-0600679 | AC-31779 | XZWQKJXJNKYMAP-UHFFFAOYSA-N | cyclohex-1-en-1-ylboronicacid | cyclohex-1-en-1-yl boronic acid | cyclohexenylboronic acid | SCHEMBL150150 | CYCLOHEX-1-ENYLBORONIC ACID | cyclohex-1-en-ylboronic acid
Specifications & Purity
≥97%
Names and Identifiers Pubchem Sid 488194617 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488194617 Canonical Smiles B(C1=CCCCC1)(O)O IUPAC Name cyclohexen-1-ylboronic acid InChIKey XZWQKJXJNKYMAP-UHFFFAOYSA-N INCHI 1S/C6H11BO2/c8-7(9)6-4-2-1-3-5-6/h4,8-9H,1-3,5H2 Isomeric SMILES B(C1=CCCCC1)(O)O Molecular Weight 125.96 Reaxy-Rn 9190670 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9190670&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 Organic acids and derivatives Class Boronic acid derivatives Subclass Boronic acids Intermediate Tree Nodes Not available Direct Parent Boronic acids Alternative Parents Organic metalloid salts Organometalloid compounds Organic oxygen compounds Hydrocarbon derivatives Molecular Framework Aliphatic homomonocyclic compounds Substituents Boronic acid - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic metalloid moeity - Aliphatic homomonocyclic compound Description 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.
3D Structure Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Melt Point(°C) 165°C Molecular Weight 125.960 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 1 Exact Mass 126.085 Da Monoisotopic Mass 126.085 Da Topological Polar Surface Area 40.500 Ų Heavy Atom Count 9 Formal Charge 0 Complexity 120.000 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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