Home > Compound List > Product Information
Bis(3,5-di-tert-butyl-4-methoxyphenyl)chlorophosphine_Molecular_structure_CAS_212713-08-1)
Click picture or here to close

Bis(3,5-di-tert-butyl-4-methoxyphenyl)chlorophosphine

Catalog No. 694703 Name Sigma Aldrich
CAS Number 212713-08-1 Website http://www.sigmaaldrich.com
M. F. C30H46ClO2P Telephone 1-800-521-8956
M. W. 505.111801 Fax
Purity Email
Storage Chembase ID: 141461

SYNONYMS

Title
二(3,5-二叔丁基-4-甲氧基苯基)氯化膦
IUPAC name
chlorobis(3,5-di-tert-butyl-4-methoxyphenyl)phosphane
IUPAC Traditional name
chlorobis(3,5-di-tert-butyl-4-methoxyphenyl)phosphane
Synonyms
Bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]phosphinous chloride

DATABASE IDS

CAS Number 212713-08-1
MDL Number MFCD08458881

PROPERTIES

Empirical Formula (Hill Notation) C30H46ClO2P
Melting Point 116-120 °C
GHS Pictograms GHS02
GHS Signal Word Warning
GHS Hazard statements H228
European Hazard Symbols Flammable Flammable (F)
MSDS Link Download
Personal Protective Equipment Eyeshields, 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
RID/ADR UN 1325 4.1/PG 3
Risk Statements 11
Hazard Class 4.1
UN Number 1325
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
100, 500 mg in glass bottle
Legal Information
Product of Kanata Chemical Technologies, Inc.
Application
Reactant for:
• Asymmetric hydrogenation with iridium catalysts1
• Condensations with optically active diols2
• Chemoselective reaction with deprotonated 2-hydoxy-3,3,N-trimethylbutanamide3Reactant for synthesis of:
• Phosphine-containing amino acids and peptide-based catalyst ligands4
• Nonracemic phosphine-containing amino acids for palladium-catalyzed asymmetric allylic substitution reactions5
Description (简体中文)
包装
100, 500 mg in glass bottle
Legal Information
Kanata Chemical Technologies, Inc. 产品
Application
Reactant for:
• Asymmetric hydrogenation with iridium catalysts1
• Condensations with optically active diols2
• Chemoselective reaction with deprotonated 2-hydoxy-3,3,N-trimethylbutanamide3Reactant for synthesis of:
• Phosphine-containing amino acids and peptide-based catalyst ligands4
• Nonracemic phosphine-containing amino acids for palladium-catalyzed asymmetric allylic substitution reactions5

REFERENCES