ChemicalBook--->CAS DataBase List--->82632-77-7

82632-77-7

82632-77-7 Structure

82632-77-7 Structure
IdentificationMore
[Name]

4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE
[CAS]

82632-77-7
[Synonyms]

CHEMBRDG-BB 3007469
4-(4-Chlorophenyl)-5-Methylthiazol-2-aMine
4-(4-chlorophenyl)-5-methyl-2-thiazolamine
4-(4-CHLOROPHENY)-5-METHYLTHIAZOL-2-YLAMINE
4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE
4-(4-chlorophenyl)-5-methyl-2-thiazol-3-idimine
4-(4-CHLOROPHENYL)-5-METHYL-1,3-THIAZOL-2-AMINE
4-(4-chlorophenyl)-5-methyl-1,3-thiazol-2-amine(SALTDATA: FREE)
[Molecular Formula]

C10H9ClN2S
[MDL Number]

MFCD00731832
[Molecular Weight]

224.71
[MOL File]

82632-77-7.mol
Chemical PropertiesBack Directory
[Melting point ]

144-145℃ (hexane ethyl acetate )
[Boiling point ]

376.6±27.0 °C(Predicted)
[density ]

1.338±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

4.43±0.10(Predicted)
[color ]

White to Yellow
[InChI]

1S/C10H9ClN2S/c1-6-9(13-10(12)14-6)7-2-4-8(11)5-3-7/h2-5H,1H3,(H2,12,13)
[InChIKey]

IEJGVSUOFMBPJU-UHFFFAOYSA-N
[SMILES]

Cc1sc(N)nc1-c2ccc(Cl)cc2
[CAS DataBase Reference]

82632-77-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

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

Xi
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[HS Code ]

2934.10.2000
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Synthesis]

4'-Chloropropiophenone

6285-05-8

Carbamimidothioic acid

17356-08-0

4-(4-CHLORO-PHENYL)-5-METHYL-THIAZOL-2-YLAMINE

82632-77-7

GENERAL METHOD: Thiourea (0.04 mol) and iodine (0.02 mol) were ground homogeneously in a mortar and subsequently mixed with 4-chloropropiophenone (0.02 mol). The reaction mixture was heated in a water bath at 70°C with intermittent stirring for 8 hours. Upon completion of the reaction, the solid product was ground to a fine powder and washed with ether to remove unreacted 4-chloropropiophenone. Next, it was washed with 5% aqueous sodium thiosulfate to remove residual iodine and finally with distilled water. The crude product was dissolved in hot water and hot filtered to remove insoluble impurities. Ammonia was slowly added to the filtrate until 2-amino-4-(4'-chlorophenyl)-5-methyl-1,3-thiazole precipitated completely. The precipitate was collected and recrystallized with ethanol to give purified crystals of the target compound [9].

[References]

[1] Asian Journal of Chemistry, 2017, vol. 29, # 12, p. 2794 - 2798
[2] Journal of the Indian Chemical Society, 1960, vol. 37, p. 427 - 428
[3] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 3, p. 313 - 317
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