Basic information Safety Supplier Related

2-Chloro-5-methylsulfanylbenzoic acid

Basic information Safety Supplier Related

2-Chloro-5-methylsulfanylbenzoic acid Basic information

Product Name:
2-Chloro-5-methylsulfanylbenzoic acid
Synonyms:
  • LABOTEST-BB LT00452880
  • 2-CHLORO-5-(METHYLTHIO)BENZOIC ACID
  • 2-CHLORO-5-METHYLSULFANYLBENZOIC ACID
  • 2-CHLORO-5-(METHYLTHIO)BENZOIC ACID TECH 98.0%
  • 2-CHLORO-5-(METHYLTHIO)BENZOIC ACID, TEC H., 96%
  • Benzoic acid, 2-chloro-5-(methylthio)-
  • Anti-CDCA3, C-Terminal antibody produced in rabbit
  • Cell division cycle-associated protein 3
CAS:
51546-12-4
MF:
C8H7ClO2S
MW:
202.66
Product Categories:
  • C8
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
51546-12-4.mol
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2-Chloro-5-methylsulfanylbenzoic acid Chemical Properties

Melting point:
136-137 °C (lit.)
Boiling point:
342.4±32.0 °C(Predicted)
Density 
1.42
storage temp. 
Sealed in dry,Room Temperature
pka
2.74±0.25(Predicted)
form 
solid
Appearance
White to off-white Solid
biological source
rabbit
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-36
WGK Germany 
3
HS Code 
2930909899

MSDS

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2-Chloro-5-methylsulfanylbenzoic acid Usage And Synthesis

Uses

2-Chloro-5-(methylthio)benzoic acid may be used in chemical synthesis studies.

Synthesis

886973-19-9

544-92-3

127510-97-8

51546-12-4

Methyl 2-chloro-5-(methylthio)benzoate (23.2 g, 106.9 mmol) and cuprous cyanide (19.2 g, 213.8 mmol) were dissolved in 100 mL of N-methylpyrrolidone. The reaction mixture was heated at 160 °C for 72 hours. The progress of the reaction was monitored by LCMS, which showed the presence of cyanide ester and hydrolyzed acid in a 1:1 ratio. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently treated with 250 mL of water and 300 mL of ethyl acetate and filtered through diatomaceous earth. After separating the organic and aqueous phases, the aqueous phase was extracted with 2 x 250 mL of ethyl acetate. The organic phases were combined, washed with 250 mL of water, dried over MgSO4 and concentrated to give an oily crude product. The crude product was purified by combi fast silica gel column chromatography using a hexane solution of 0-20% ethyl acetate as eluent, resulting in methyl 2-cyano-5-(methylthio)benzoate (6.14 g, 28% yield) as a white solid.The LCMS analysis showed the following: retention time (Rt) = 2.42 min; mass-to-charge ratio (m/z) [M + H]+ = 208.

References

[1] Patent: WO2006/67462, 2006, A1. Location in patent: Page/Page column 61

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