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About This Item
Linear Formula:
CH3COCH2P(Cl)(C6H5)3
CAS Number:
Molecular Weight:
354.81
EC Number:
214-974-1
UNSPSC Code:
12352107
PubChem Substance ID:
Beilstein/REAXYS Number:
3922783
MDL number:
assay
98%
form
solid
reaction suitability
reaction type: C-C Bond Formation
mp
243-245 °C (lit.)
SMILES string
[Cl-].CC(=O)C[P+](c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C21H20OP.ClH/c1-18(22)17-23(19-11-5-2-6-12-19,20-13-7-3-8-14-20)21-15-9-4-10-16-21;/h2-16H,17H2,1H3;1H/q+1;/p-1
InChI key
XAMZZEBAJZJERT-UHFFFAOYSA-M
Application
Used to investigate the antimycobacterial activities of Me alkenyl quinolones
Reactant for synthesis of:
Reactant for Wittig olefinations
Reactant for synthesis of:
- Unsaturated esters and ketones containing multiple aromatic and heteroaromatic rings using Suzuki coupling - Wittig olefination
- Fused oxygen and nitrogen heterocycles via regioselective cyclocondensation
Reactant for Wittig olefinations
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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