ChemicalBook--->CAS DataBase List--->21734-85-0

21734-85-0

21734-85-0 Structure

21734-85-0 Structure
IdentificationBack Directory
[Name]

5-CHLORO-3-METHYL-1,2,4-THIADIAZOLE
[CAS]

21734-85-0
[Synonyms]

5-chloro-3-methyl-1,2,4-thiazole
5-Chlor-3-methyl-[1,2,4]thiadiazol
5-CHLORO-3-METHYL-1,2,4-THIADIAZOLE
1,2,4-Thiadiazole, 5-chloro-3-methyl-
[Molecular Formula]

C3H3ClN2S
[MDL Number]

MFCD08234803
[MOL File]

21734-85-0.mol
[Molecular Weight]

134.59
Chemical PropertiesBack Directory
[Boiling point ]

51 °C(Press: 21 Torr)
[density ]

1.355 g/cm3
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

liquid
[pka]

0.36±0.10(Predicted)
[color ]

Pale yellow
[InChI]

1S/C3H3ClN2S/c1-2-5-3(4)7-6-2/h1H3
[InChIKey]

ILTLLMVRPBXCSX-UHFFFAOYSA-N
[SMILES]

ClC1=NC(C)=NS1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280-P271
[Hazard Codes ]

Xi
[Risk Statements ]

41
[Safety Statements ]

26-39
[WGK Germany ]

WGK 3
[HS Code ]

2934999090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Spectrum DetailBack Directory
[Spectrum Detail]

5-CHLORO-3-METHYL-1,2,4-THIADIAZOLE(21734-85-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Acetamidine hydrochloride

124-42-5

Perchloromethylmercaptan

594-42-3

5-CHLORO-3-METHYL-1,2,4-THIADIAZOLE

21734-85-0

The general procedure for the synthesis of 5-chloro-3-methyl-1,2,4-thiadiazole from acetamidine hydrochloride and perchloromethylmercaptan was as follows: to a stirred mixture of acetamidine hydrochloride (38.1 g, 0.40 mol) and trichloromethanesulfonyl chloride (75 g, 0.40 mol) at ±5°C, an aqueous solution containing NaOH (75.7 g, 0.40 mol) was slowly added dropwise (126mL). After the dropwise addition, the reaction mixture was stirred at 0°C for 30 minutes and then allowed to warm up to room temperature. After completion of the reaction, the mixture was filtered and the layers were separated. The aqueous phase was extracted with dichloromethane (3 x 150 mL). All organic phases were combined and washed with brine (2 x 150 mL) and subsequently dried with anhydrous magnesium sulfate. Finally, the solvent was removed under reduced pressure to afford the target product 5-chloro-3-methyl-1,2,4-thiadiazole (43 g, 83% yield) as a dark colored oil.

[References]

[1] Patent: US2010/160392, 2010, A1. Location in patent: Page/Page column 18
[2] Patent: WO2007/100670, 2007, A1. Location in patent: Page/Page column 48
[3] Patent: WO2005/7636, 2005, A1. Location in patent: Page/Page column 14; 15
[4] Journal of Medicinal Chemistry, 2002, vol. 45, # 9, p. 1887 - 1900
[5] Chemische Berichte, 1957, vol. 90, p. 182,186
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