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· · COA & SDS available for every product · Same-day shipping on in-stock items Isopropylboronic Acid (contains varying amounts of Anhydride) - ≥97% , CAS No.80041-89-0
Synonyms
isopropylboric acid | I0787 | Boronic acid, B-(1-methylethyl)- | DTXSID90370481 | A839820 | (Propan-2-yl)boronic acid | Boronic acid, (1-methylethyl)- | 2-Propaneboronic acid | SY006229 | GS-6619 | propan-2-ylboronic acid | FT-0647396 | AKOS005146521 | Is
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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.
Overview Reactant or reagent involved in: 1.Copper-promoted cross-coupling. 2.Domino Heck-Suzuki reactions. 3.C-H activation for arylations and alkylations. 4.Suzuki-Miyaura type couple reactions. 5.Alkylation-hydride reduction sequence.
Specifications Synonyms
isopropylboric acid | I0787 | Boronic acid, B-(1-methylethyl)- | DTXSID90370481 | A839820 | (Propan-2-yl)boronic acid | Boronic acid, (1-methylethyl)- | 2-Propaneboronic acid | SY006229 | GS-6619 | propan-2-ylboronic acid | FT-0647396 | AKOS005146521 | Is
Specifications & Purity
≥97%
Names and Identifiers Canonical Smiles B(C(C)C)(O)O IUPAC Name propan-2-ylboronic acid InChIKey QIPHSSYCQCBJAX-UHFFFAOYSA-N INCHI 1S/C3H9BO2/c1-3(2)4(5)6/h3,5-6H,1-2H3 Isomeric SMILES B(C(C)C)(O)O WGK Germany 3 Molecular Weight 87.91 Beilstein 4(4)4382 Reaxy-Rn 1731883 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1731883&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 Organic oxygen compounds Monoalkylboranes Hydrocarbon derivatives Molecular Framework Aliphatic acyclic compounds Substituents Boronic acid - Organic metalloid salt - Organic oxygen compound - Monoalkylborane - Alkylborane - Hydrocarbon derivative - Organic salt - Organoboron compound - Aliphatic acyclic 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 Sensitivity Hygroscopic Melt Point(°C) 95-100°C Molecular Weight 87.920 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 1 Exact Mass 88.0696 Da Monoisotopic Mass 88.0696 Da Topological Polar Surface Area 40.500 Ų Heavy Atom Count 6 Formal Charge 0 Complexity 35.800 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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