158070
2-Oxopropyltriphenylphosphonium chloride
98%
Synonym(s):
Acetonyltriphenylphosphonium chloride
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About This Item
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
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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 Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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