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About This Item
Linear Formula:
(CH3)3CPCl2
CAS Number:
Molecular Weight:
158.99
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352001
EC Number:
247-386-9
MDL number:
Quality Level
assay
98%
reaction suitability
reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling
mp
44-49 °C (lit.)
functional group
phosphine
SMILES string
CC(C)(C)P(Cl)Cl
InChI
1S/C4H9Cl2P/c1-4(2,3)7(5)6/h1-3H3
InChI key
NMJASRUOIRRDSX-UHFFFAOYSA-N
Application
tert-Butyldichlorophosphine can be used as a reactant for the synthesis of:
- Dihydrobenzooxaphosphole core.
- tert-Butyl functionalized 1,3-C6H4(CH2PR2)2 (PCP) pincer ligands.
- Chloro-phosphinite reagent by reacting with sodium ethoxide.
- 2-(tert-Butylhydrophosphoryl)-1-phenyl-1H-imidazole derivatives.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
supp_hazards
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Imidazolio-substituted secondary phosphine oxides as potential carbene reagents.
Chang YC, et al.
Polyhedron, 100(19-20), 382-391 (2015)
Synthesis and coordination chemistry of new asymmetric donor/acceptor pincer ligands, 1, 3-C6H4 (CH2PtBu(Rf))2 (Rf= CF3, C2F5).
Debnath S, et al.
Dalton Transactions, 47(35), 12420-12430 (2018)
Solid-phase synthesis and catalytic screening of polystyrene supported diphosphines.
Samuels MC, et al.
Topics in Catalysis, 59(19-20), 1793-1799 (2016)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 381020-10G | 04061833547205 |
