Sign Into View Organizational & Contract Pricing
About This Item
Linear Formula:
[(CH3)3C]2PCl
CAS Number:
Molecular Weight:
180.66
MDL number:
UNSPSC Code:
12352001
PubChem Substance ID:
Product Name
Di-tert-butylchlorophosphine, 96%
Quality Level
assay
96%
form
liquid
reaction suitability
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling
refractive index
n20/D 1.482 (lit.)
bp
48 °C/3 mmHg (lit.)
density
0.951 g/mL at 25 °C (lit.)
functional group
phosphine
SMILES string
CC(C)(C)P(Cl)C(C)(C)C
InChI
1S/C8H18ClP/c1-7(2,3)10(9)8(4,5)6/h1-6H3
InChI key
MCRSZLVSRGTMIH-UHFFFAOYSA-N
General description
Di-tert-butylchlorophosphine belongs to the class of phosphine ligands. It is used for cross-coupling reactions because of the flexibility of its electronic and steric properties. It plays a key role in stabilizing and activating the central metal atom and is used in reactions such as transition metal-catalyzed C-O, C-N, and C-C bond-forming reactions.
Application
Di-tert-butylchlorophosphine can be used as a ligand in:
- The Pd-catalyzed amination reaction with aryl halides.
- The Pd-catalyzed Suzuki-Miyaura cross-coupling of arylboronic acids with aryl bromides and chlorides.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
143.6 °F - closed cup
flash_point_c
62 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service