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2-Chloro-3-methylbenzoic acid

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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
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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)
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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
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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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