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Dibromoborane dimethyl sulfide complex_Molecular_structure_CAS_55671-55-1)
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Dibromoborane dimethyl sulfide complex

Catalog No. 255106 Name Sigma Aldrich
CAS Number 55671-55-1 Website http://www.sigmaaldrich.com
M. F. C2H7BBr2S Telephone 1-800-521-8956
M. W. 233.76098 Fax
Purity Email
Storage Chembase ID: 149114

SYNONYMS

Title
二溴硼烷甲硫醚络合物
IUPAC name
(methylsulfanyl)methane; dibromoborane
IUPAC Traditional name
dibromoborane; dimethyl sulfide
Synonyms
二溴甲基硫醚化硼络合物
Dibromoborane dimethyl sulfide
Dibromo(dimethyl sulfide)(hydro)boron
Dibromo(dimethyl sulfide)borane
Dibromoborane compound with dimethylsulfane
Boron dibromide methyl sulfide complex

DATABASE IDS

MDL Number MFCD00011601
Beilstein Number 4449985
CAS Number 55671-55-1
PubChem SID 24855287

PROPERTIES

Linear Formula (CH3)2S · BHBr2
Flash Point 26 °C
Flash Point 78.8 °F
Melting Point 30-35 °C(lit.)
GHS Pictograms GHS02
GHS Pictograms GHS05
GHS Signal Word Danger
GHS Hazard statements H228-H261-H314
European Hazard Symbols Corrosive Corrosive (C)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
GHS Precautionary statements P210-P231 + P232-P280-P305 + P351 + P338-P310-P422
RID/ADR UN 3396 4.3/PG 2
Risk Statements 10-14/15-34
Safety Statements 16-26-36/37/39-45
Supplemental Hazard Statements Reacts violently with water.
Hazard Class 4.3
UN Number 3396
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Packaging
100 g in Sure/Seal™
Application
Reactant for:
• Reductive elimination C-C bond forming reactions1
• Lithiation-borylation reaction with Hoppe′s lithiated carbamates2
• Preparation of boron analogues of uracil3
• Boronation reactions for formation of cyclic boronium salts4
• Hydroboration reactions5
• Ring opening of terminal epoxides6
Description (简体中文)
包装
100 g in Sure/Seal™
Application
Reactant for:
• Reductive elimination C-C bond forming reactions1
• Lithiation-borylation reaction with Hoppe′s lithiated carbamates2
• Preparation of boron analogues of uracil3
• Boronation reactions for formation of cyclic boronium salts4
• Hydroboration reactions5
• Ring opening of terminal epoxides6

REFERENCES