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Acetylthiomethyl-diphenylphosphine borane complex_Molecular_structure_CAS_446822-71-5)
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Acetylthiomethyl-diphenylphosphine borane complex

Catalog No. 670359 Name Sigma Aldrich
CAS Number 446822-71-5 Website http://www.sigmaaldrich.com
M. F. C15H18BOPS Telephone 1-800-521-8956
M. W. 288.152581 Fax
Purity ≥98.0% Email
Storage Chembase ID: 141003

SYNONYMS

Title
乙酰基硫甲基-硼烷二苯基膦复合物
IUPAC name
1-{[(diphenylphosphanyl)methyl]sulfanyl}ethan-1-one borane
IUPAC Traditional name
1-{[(diphenylphosphanyl)methyl]sulfanyl}ethanone borane

DATABASE IDS

CAS Number 446822-71-5

PROPERTIES

Empirical Formula (Hill Notation) C15H18BOPS
Purity ≥98.0%
Melting Point 52-55 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26
Storage Temperature 2-8°C
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
250 mg in glass bottle
Legal Information
Sold under license for research and development purposes only. US Patent 6,974,884 and related patents apply
Application

• Traceless Staudinger ligation reagent with borane protecting group.
• The borane group stabilizes the phosphine against oxidation and can be easily removed with mild basic or acidic conditions to yield the active phosphine.1
• After reaction with an azide, the phosphine is eliminated in the presence of water to yield a native amide bond.2
• Used in the synthesis of cyclic peptides.2
Description (简体中文)
包装
1 g in glass bottle
250 mg in glass bottle
Legal Information
授权后方可销售,仅供研发使用。美国专利 6,974,884 和相关专利申请
Application

• Traceless Staudinger ligation reagent with borane protecting group.
• The borane group stabilizes the phosphine against oxidation and can be easily removed with mild basic or acidic conditions to yield the active phosphine.1
• After reaction with an azide, the phosphine is eliminated in the presence of water to yield a native amide bond.2
• Used in the synthesis of cyclic peptides.2

REFERENCES