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trans-1-Octen-1-ylboronic acid_Molecular_structure_CAS_42599-16-6)
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trans-1-Octen-1-ylboronic acid

Catalog No. 521027 Name Sigma Aldrich
CAS Number 42599-16-6 Website http://www.sigmaaldrich.com
M. F. C8H17BO2 Telephone 1-800-521-8956
M. W. 156.03038 Fax
Purity Email
Storage Chembase ID: 10788

SYNONYMS

Title
反式-1-辛烯-1-基硼酸
IUPAC name
[(1E)-oct-1-en-1-yl]boronic acid
IUPAC Traditional name
(1E)-oct-1-en-1-ylboronic acid
Synonyms
(E)-1-Octenylboronic acid
trans-1-Octenylboronic acid
(2E)-2-Octen-1-ylboronic acid
(E)-1-Octen-1-ylboronic acid

DATABASE IDS

PubChem SID 24874184
MDL Number MFCD02093734
CAS Number 42599-16-6

PROPERTIES

Linear Formula CH3(CH2)5CH=CHB(OH)2
Melting Point 100-104 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Other Notes
Contains varying amounts of anhydride
Packaging
1 g in glass bottle
Application
Reactant for:
• Chiral palladacycle-catalyzed asymmetric ring-opening reaction1
• Enantioselective conjugate addition catalyzed by acyltartaric acids2
• Copper-mediated oxidative cross-coupling reactions3
• Diastereoselective domino Heck-Suzuki reactions4
Description (简体中文)
Other Notes
含不定量的酸酐
包装
1 g in glass bottle
Application
Reactant for:
• Chiral palladacycle-catalyzed asymmetric ring-opening reaction1
• Enantioselective conjugate addition catalyzed by acyltartaric acids2
• Copper-mediated oxidative cross-coupling reactions3
• Diastereoselective domino Heck-Suzuki reactions4

REFERENCES