Weight | 172.567 g/mol |
---|---|
Formula | C7H5ClO3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3-Chloroperoxybenzoic acid (937-14-4)
MCPBA · m-chloroperbenzoic acid · m-CPBA
Score:
#4202 in Chemistry
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- Iodobenzene-catalyzed alpha-acetoxylation of ketones. in situ generation of hypervalent (diacyloxyiodo)benzenes using m-chloroperbenzoic acid. (Journal of the American Chemical Society, 2005)
- Versatile Hypervalent-Iodine(III)-Catalyzed Oxidations with m-Chloroperbenzoic Acid as a Cooxidant (Angewandte Chemie, 2005)
- Epoxidations with m-Chloroperbenzoic Acid (Journal of Organic Chemistry, 1964)
- Evidence for Compound I Formation in the Reaction of Cytochrome-P450cam with m-Chloroperbenzoic Acid (Biochemical and Biophysical Research Communications, 1994)
- m-Chloroperbenzoic acid oxidation of 2-trimethylsilyloxy-1,3-dienes. Synthesis of .alpha.-hydroxy and .alpha.-acetoxy enones (Journal of Organic Chemistry, 1978)
- Nitroxide-catalyzed oxidation of alcohols using m-chloroperbenzoic acid. New method (Journal of Organic Chemistry, 1975)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - MCPBA
- m-chloroperbenzoic acid
- m-CPBA
- meta-chloroperoxybenzoic acid
- 3-chloroperbenzoic acid
-
SMILESC1=CC(=CC(=C1)Cl)C(=O)OO
-
InChIKeyNHQDETIJWKXCTC-UHFFFAOYSA-N
- Pubchem - 3-Chloroperoxybenzoic acid
- Wikipedia - 3-chloroperbenzoic acid
meta-Chloroperoxybenzoic acid (mCPBA) is a peroxycarboxylic acid used widely as an oxidant in organic synthesis. mCPBA is often preferred to other peroxy acids because of its relative ease of handling. The main areas of use are the conversion of ketones to esters (Baeyer-Villiger oxidation), epoxidation of alkenes (Prilezhaev reaction), conversion of silyl enol ethers to silyl -hydroxy ketones (Rubottom oxidation), oxidation of sulfides to sulfoxides and sulfones, and oxidation of amines to produce amine oxides.
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Similar Compounds
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3,5-DICHLOROBENZOIC ACID
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3-Chloro-4-methylbenzoic acid
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3,4-DICHLOROBENZOIC ACID
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5-Chloroisophthalic acid
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3,5-Dichloro-4-methylbenzoic acid
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3,4,5-Trichlorobenzoic acid
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Methyl 3,5-dichlorobenzoate
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5-Chloro-2-methylbenzoic acid
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2,5-DICHLOROBENZOIC ACID
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3-CHLORO-4-HYDROXYBENZOIC ACID
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4-AMINO-3-CHLOROBENZOIC ACID
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Methyl 3,4-dichlorobenzoate
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3-Chloro-2-methylbenzoic acid
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Dimethyl 5-chloroisophthalate
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3-Bromo-5-chlorobenzoic acid
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2,5-Dichloroterephthalic acid
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3-CHLOROBENZALDEHYDE
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4-bromo-3,5-dichlorobenzoic acid
(117738-75-7)
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2-Bromo-5-chlorobenzoic acid
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2,3-DICHLOROBENZOIC ACID
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4-Chloro-2-methylbenzoic acid
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3-Chlorobenzyl alcohol
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3,5-Dichloro-4-hydroxybenzoic acid
(3336-41-2)
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4-AMINO-3,5-DICHLOROBENZOIC ACID
(56961-25-2)
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5-Chloro-2-iodobenzoic acid
(13421-00-6)
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3-Chloro-4-methoxybenzoic acid
(37908-96-6)
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5-CHLOROSALICYLIC ACID
(321-14-2)
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3,5-Dichlorobenzaldehyde
(10203-08-4)
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2-AMINO-5-CHLOROBENZOIC ACID
(635-21-2)
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4-Chloro-3-methylbenzoic acid
(7697-29-2)
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2,4,5-TRICHLOROBENZOIC ACID
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(26264-09-5, 118-91-2)
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Methyl 4-amino-3-chlorobenzoate
(84228-44-4)
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2,3,5-Trichlorobenzoic acid
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METHYL 2,5-DICHLOROBENZOATE
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2 safety hazards
3 suppliers
3,5-DICHLOROBENZYL ALCOHOL
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2-bromo-3-chlorobenzoic acid
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3,4-Dichlorobenzoic anhydride
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Methyl 4-chlorobenzoate
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3-Chloro-4-methylbenzyl alcohol
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Dimethyl 2-chloroterephthalate
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3,4-DICHLOROBENZALDEHYDE
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3,5-dichloro-4-methoxybenzoic acid
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29605-78-5
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Ethyl 2,5-dichlorobenzoate
(35112-27-7)
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(3337-59-5)
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Chlorthal
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3,4-Dichlorobenzyl alcohol
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2,5-Dichlorobenzaldehyde
(6361-23-5)
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60088-54-2
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