2-Chloro-3-methylbenzoic acid
2-Chloro-3-methylbenzoic acid Basic information
- Product Name:
- 2-Chloro-3-methylbenzoic acid
- Synonyms:
-
- 2-CHLORO-3-METHYLBENZOIC ACID
- 2-CHLORO-M-TOLUIC ACID
- 3-methyl-2-chlorobenzoic acid
- 2-CHLORO-3-METHYLBENZOIC ACID 98%
- 2-Chloro-3-Methyl
- 2-Chloro-3-methylben
- 2-Chloro-3-methylbenzoic Acid >
- Benzoic acid, 2-chloro-3-methyl-
- CAS:
- 15068-35-6
- MF:
- C8H7ClO2
- MW:
- 170.59
- Product Categories:
-
- Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
- Benzoic acid
- Organic acids
- Acids & Esters
- Chlorine Compounds
- Mol File:
- 15068-35-6.mol
2-Chloro-3-methylbenzoic acid Chemical Properties
- Melting point:
- 142-144°C
- Boiling point:
- 288.7±20.0 °C(Predicted)
- Density
- 1.310±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- form
- powder to crystal
- pka
- 3.08±0.25(Predicted)
- color
- White to Light yellow to Light orange
- CAS DataBase Reference
- 15068-35-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36/37/38-41-22
- Safety Statements
- 26-36/37/39-39
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 2916399090
2-Chloro-3-methylbenzoic acid Usage And Synthesis
Chemical Properties
Off-white powder
Uses
2-Chloro-3-methylbenzoic acid can be used in organic synthesis and experimental research.
Chemical Reactivity
2-Chloro-3-methylbenzoic acid is stable under proper conditions, it reacts with oxidizing agents.
Synthesis
6781-98-2
13049-16-6
15068-35-6
General procedure for the synthesis of 2-chloroisophthalic acid and 2-chloro-3-methylbenzoic acid from 2,6-dimethylchlorobenzene: In a reaction system, 140 g of 2,6-dimethylchlorobenzene, 0.14 g of Co(OAc)2, 0.14 g of NaBr, and 14 g of acetic acid were added, and the system was heated to 95 °C with stirring until the catalyst was completely dissolved. 64 g of atmospheric pressure was introduced into the system and maintained for 6.7 hours. Sample tests were performed during the reaction and showed that 20% of the feedstock 2,6-dimethylchlorobenzene remained, 40% of the product 2-chloro-3-methylbenzoic acid, 30% of 2,6-dicarboxychloride, 5% of 2-chloro-3-carboxybenzaldehyde, and 5% of 2-chloro-3-methylbenzaldehyde. After completion of the reaction, the reaction solution was cooled to room temperature. After post-treatment, the solid product 2-chloro-3-methylbenzoic acid was obtained in 30% yield.
References
[1] Patent: CN108530297, 2018, A. Location in patent: Paragraph 0103; 0104
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