Weight | 170.595 g/mol |
---|---|
Formula | C8H7ClO2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
4-Chlorophenylacetic acid (1878-66-6)
4-chlorophenylacetate · 4-chlorophenylacetic acid, potassium salt · 4-chlorophenylacetic acid, sodium salt
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- Purification and some properties of component B of the 4-chlorophenylacetate 3,4-dioxygenase from Pseudomonas species strain CBS 3. (Journal of Biological Chemistry, 1987)
- Oxidation and dehalogenation of 4-chlorophenylacetate by a two-component enzyme system from Pseudomonas sp. strain CBS3. (Journal of Bacteriology, 1984)
- Degradation of 4-chlorophenylacetic acid by a Pseudomonas species. (Journal of Bacteriology, 1981)
- Pharmacology of a new analgesic, antipyretic, and anti-inflammatory agent, 4-allyloxy-3-chlorophenylacetic acid. (Drug Research, 1970)
- Asymmetric catalytic alkylation of 4-chlorophenylacetic acid (Tetrahedron-asymmetry, 1993)
- 4-Allyloxy-3-chlorophenylacetic acid, a new type of analgesic, antipyretic and antiphlogistic drug (Naturwissenschaften, 1969)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-chlorophenylacetate
- 4-chlorophenylacetic acid, potassium salt
- 4-chlorophenylacetic acid, sodium salt
-
SMILESC1=CC(=CC=C1CC(=O)O)Cl
-
InChIKeyCDPKJZJVTHSESZ-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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