273031
3-Chloroperbenzoic acid
≤77%
동의어(들):
meta-Chloroperbenzoic acid, 3-Chloroperoxybenzoic acid, MCPBA
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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
ClC6H4CO3H
CAS 번호:
Molecular Weight:
172.57
UNSPSC Code:
12352302
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
608317
Assay:
≤77%
Form:
solid
Quality Level
assay
≤77%
form
solid
reaction suitability
reagent type: oxidant
mp
69-71 °C (lit.)
functional group
chloro, hydroperoxide
storage temp.
2-8°C
SMILES string
OOC(=O)c1cccc(Cl)c1
InChI
1S/C7H5ClO3/c8-6-3-1-2-5(4-6)7(9)11-10/h1-4,10H
InChI key
NHQDETIJWKXCTC-UHFFFAOYSA-N
General description
3-Chloroperbenzoic acid is a strong oxidizing agent mainly used for the epoxidation of alkenes and also in the Baeyer-Villiger oxidation of ketones to esters.
Application
Effective oxidant for epoxidizing di-, tri-, and tetra-substituted olefins.
3-Chloroperbenzoic acid has been used in the oxidation of N-p-tolylsulfinyl-(E)-1-phenylethylideneimine to N-p-tolylsulfonyl (E)-1-phenylethylideneimine using dichloromethane as a solvent. It has also been used in the preparation of mono- and di-epoxy-functionalized poly(3-hydroxybutyrate)-based reactive polymers. MCPBA is also an effective oxidizing agent for conversion of α-amide substituted polyesters to their corresponding polysulfones with tunable thermal properties.
Other Notes
remainder 3-chlorobenzoic acid and water
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Org. Perox. D - Skin Corr. 1C - Skin Sens. 1
저장 등급
5.2 - Organic peroxides and self-reacting 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
문서
The Baeyer-Villiger oxidation is the oxidative cleavage of a carbon-carbon bond adjacent to a carbonyl, which converts the ketones to esters and the cyclic ketones to lactones.
Chiral Mn (III) salen complexes covalently bonded on modified MCM-41 and SBA-15 as efficient catalysts for enantioselective epoxidation of nonfunctionalized alkenes.
Kureshy R
J. Catal., 238(1), 134-141 (2006)
Rearrangements of organic peroxides and related processes.
Yaremenko I
Beilstein Journal of Organic Chemistry, 12, 1647-1647 (2016)
Preparation of N?p?Tolylsulfonyl?(E)?1?Phenylethylideneimine.
Ruano J
Organic Syntheses, 129-138 (2007)