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51546-12-4

51546-12-4 Structure

51546-12-4 Structure
IdentificationBack Directory
[Name]

2-Chloro-5-methylsulfanylbenzoic acid
[CAS]

51546-12-4
[Synonyms]

TOME-1
LABOTEST-BB LT00452880
Gene-rich cluster protein C8
Trigger of mitotic entry protein 1
2-CHLORO-5-(METHYLTHIO)BENZOIC ACID
2-CHLORO-5-METHYLSULFANYLBENZOIC ACID
Benzoic acid, 2-chloro-5-(methylthio)-
Cell division cycle-associated protein 3
2-CHLORO-5-(METHYLTHIO)BENZOIC ACID TECH 98.0%
2-CHLORO-5-(METHYLTHIO)BENZOIC ACID, TEC H., 96%
Anti-CDCA3, C-Terminal antibody produced in rabbit
2-Chloro-5-(Methylthio)benzoic acid technical grade, 96%
3-Carboxy-4-chlorothioanisole, 2-Chloro-5-(methylsulphanyl)benzoic acid
[Molecular Formula]

C8H7ClO2S
[MDL Number]

MFCD00009721
[MOL File]

51546-12-4.mol
[Molecular Weight]

202.66
Chemical PropertiesBack Directory
[Melting point ]

136-137 °C (lit.)
[Boiling point ]

342.4±32.0 °C(Predicted)
[density ]

1.42
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

2.74±0.25(Predicted)
[Appearance]

White to off-white Solid
[biological source]

rabbit
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37/39-36
[WGK Germany ]

3
[HS Code ]

2930909899
Hazard InformationBack Directory
[Uses]

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

Benzoic acid, 2-chloro-5-(methylthio)-, methyl ester

886973-19-9

Copper(I) Cyanide

544-92-3

Benzoic acid, 2-cyano-5-(methylthio)-, methyl ester

127510-97-8

2-Chloro-5-methylsulfanylbenzoic acid

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
Spectrum DetailBack Directory
[Spectrum Detail]

2-Chloro-5-methylsulfanylbenzoic acid(51546-12-4)MS
2-Chloro-5-methylsulfanylbenzoic acid(51546-12-4)1HNMR
2-Chloro-5-methylsulfanylbenzoic acid(51546-12-4)13CNMR
2-Chloro-5-methylsulfanylbenzoic acid(51546-12-4)IR1
2-Chloro-5-methylsulfanylbenzoic acid(51546-12-4)IR2
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