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trans-1-Propen-1-ylboronic acid_Molecular_structure_CAS_7547-97-9)
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trans-1-Propen-1-ylboronic acid

Catalog No. 576638 Name Sigma Aldrich
CAS Number 7547-97-9 Website http://www.sigmaaldrich.com
M. F. C3H7BO2 Telephone 1-800-521-8956
M. W. 85.89748 Fax
Purity ≥95.0% Email
Storage Chembase ID: 144646

SYNONYMS

Title
反丙烯硼酸
IUPAC name
[(1E)-prop-1-en-1-yl]boronic acid
IUPAC Traditional name
(1E)-prop-1-en-1-ylboronic acid
Synonyms
trans-1-Propenylboronic acid
(E)-Prop-1-enylboronic acid
(E)-1-Propen-1-ylboronic acid
trans-1-Propeneboronic acid
trans-Propenylboronic acid

DATABASE IDS

PubChem SID 24880870
MDL Number MFCD02179501
CAS Number 7547-97-9

PROPERTIES

Impurities ~10 wt. % cis-isomer
Linear Formula CH3CH=CHB(OH)2
Purity ≥95.0%
Melting Point 123-127 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions1,2
• Cu(II)-mediated Ullmann-type coupling3Reactant for preparation of:
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases4
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling5
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization6
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones7
Reactant for
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions1,2
• Cu(II)-mediated Ullmann-type coupling3
• Palladium-catalyzed Sonogashira cross-coupling7 Reactant for preparation of
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases4
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling5
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones
Description (简体中文)
Frequently Asked Questions
Live Chat and Frequently Asked Questions are available for this Product.
Other Notes
含有不定量的酸酐
包装
1, 5 g in glass bottle
Application
Reactant for:
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions1,2
• Cu(II)-mediated Ullmann-type coupling3Reactant for preparation of:
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases4
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling5
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization6
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones7
Reactant for
• Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions1,2
• Cu(II)-mediated Ullmann-type coupling3
• Palladium-catalyzed Sonogashira cross-coupling7 Reactant for preparation of
• Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases4
• Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling5
• Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization
• Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones

REFERENCES