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ChemicalBook--->CAS DataBase List--->72605-86-8

72605-86-8

72605-86-8 Structure

72605-86-8 Structure
IdentificationBack Directory
[Name]

methyl 2-chlorothiazole-5-carboxylate
[CAS]

72605-86-8
[Synonyms]

5-Carbomethoxy-2-chlorothiazole
Methyl 2-chloro-5-thiazolecarboxylate
2-Chloro-5-(methoxycarbonyl)-1,3-thiazole
Methyl 2-chlorothiazole-5-carboxylate 97%
2-Chloro-5-thiazolecarboxylic acid methyl ester
2-Chlorothiazole-5-carboxylic acid methyl ester
2-Chloro-thiazole-5-Carbocylic acid methyl ester
5-Thiazolecarboxylic acid, 2-chloro-, Methyl ester
[EINECS(EC#)]

812-581-5
[Molecular Formula]

C5H4ClNO2S
[MDL Number]

MFCD09265500
[MOL File]

72605-86-8.mol
[Molecular Weight]

177.61
Chemical PropertiesBack Directory
[Boiling point ]

271.2±32.0 °C(Predicted)
[density ]

1.456±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

powder
[pka]

-1.09±0.10(Predicted)
[color ]

White
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2934100090
Spectrum DetailBack Directory
[Spectrum Detail]

methyl 2-chlorothiazole-5-carboxylate(72605-86-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Thiazolecarboxylic acid, 2-amino-, methyl ester, hydrochloride (1:1)

726185-57-5

methyl 2-chlorothiazole-5-carboxylate

72605-86-8

A suspension was prepared from methyl 2-aminothiazole-5-carboxylate hydrochloride (14.0 g, 71.927 mmol) in 8 ml of concentrated hydrochloric acid to which 20 g of crushed ice was added. An aqueous solution (30 ml) of sodium nitrite (5.0 g, 72.464 mmol) was added slowly and dropwise under external cooling conditions, ensuring that the reaction temperature was maintained below 0 °C at all times. After 30 min of reaction, copper(I) chloride (7.2 g, 72.735 mmol) was added and stirring was continued under cooling conditions for 1 h, followed by a slow warming up to room temperature over 1.5 h. The reaction was completed with the addition of ether. After completion of the reaction, the reaction mixture was thoroughly extracted with ether, the organic phases were combined, washed with saturated brine solution, dried over anhydrous sodium sulfate and the solvent was subsequently evaporated. Methyl 2-chlorothiazole-5-carboxylate 4.3 g (34% yield) was obtained as a colorless oil with a thin layer chromatographic Rf value of 0.94 (Unfolding agent: EI D). The product was used directly in the next reaction without further purification. Mass spectrometry analysis showed the molecular ion peak M+ = 177/179 (Cl isotope peak).

[References]

[1] Patent: US2004/192729, 2004, A1. Location in patent: Page 34
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