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Chlorodicyclohexylborane solution_Molecular_structure_CAS_36140-19-9)
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Chlorodicyclohexylborane solution

Catalog No. 411124 Name Sigma Aldrich
CAS Number 36140-19-9 Website http://www.sigmaaldrich.com
M. F. C12H22BCl Telephone 1-800-521-8956
M. W. 212.56708 Fax
Purity Email
Storage Chembase ID: 136834

SYNONYMS

Title
氯代二环己基硼烷 溶液
IUPAC name
chlorodicyclohexylborane
IUPAC Traditional name
chlorodicyclohexylborane
Synonyms
Dicyclohexylboron chloride
Dicyclohexylboryl chloride
Dicyclohexylchloroborane
氯化二环己基硼烷

DATABASE IDS

MDL Number MFCD00191906
CAS Number 36140-19-9
Beilstein Number 3233942
PubChem SID 24865728

PROPERTIES

Concentration 1 M in hexanes
Linear Formula (C6H11)2BCl
Boiling Point 68-69 °C
Density 0.752 g/mL at 25 °C
Flash Point -12 °C
Flash Point 10.4 °F
GHS Pictograms GHS02
GHS Pictograms GHS05
GHS Pictograms GHS07
GHS Pictograms GHS08
GHS Pictograms GHS09
GHS Signal Word Danger
GHS Hazard statements H225-H250-H304-H314-H336-H361f-H373-H411
European Hazard Symbols Flammable Flammable (F)
European Hazard Symbols Corrosive Corrosive (C)
European Hazard Symbols Nature polluting Nature polluting (N)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P210-P222-P231-P261-P273-P422
RID/ADR UN 2924 3/PG 2
Risk Statements 11-17-34-48/20-51/53-62-65-67
Safety Statements 16-26-36/37/39-45-61-62
Hazard Class 3
UN Number 2924
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Packaging
50, 100 mL in Sure/Seal™
Application
Reactant for:
• Aldol addition reactions1
• Mukaiyama aldol addition2
• Microwave assisted ring closing metathesis reactions3
• C-alkylation of aromatic aldimines4
• Reversible ketone-ketone aldol reactions5
• Syn- and anti-stereoselective aldol reaction hexenone with aldehydes6
Description (简体中文)
包装
50, 100 mL in Sure/Seal™
Application
Reactant for:
• Aldol addition reactions1
• Mukaiyama aldol addition2
• Microwave assisted ring closing metathesis reactions3
• C-alkylation of aromatic aldimines4
• Reversible ketone-ketone aldol reactions5
• Syn- and anti-stereoselective aldol reaction hexenone with aldehydes6

REFERENCES