ChemicalBook--->CAS DataBase List--->828-81-9

828-81-9

828-81-9 Structure

828-81-9 Structure
IdentificationBack Directory
[Name]

2-AMINO-5-(2-CHLOROPHENYL)-1,3,4-THIADIAZOLE
[CAS]

828-81-9
[Synonyms]

VITAS-BB TBB000090
5-(2-Chlorophenyl)
IFLAB-BB F1386-0067
5-(2-CHLOROPHENYL)-1,3,4-THIADIAZOL-2-AMINE
2-AMINO-5-(2-CHLOROPHENYL)-1,3,4-THIADIAZOLE
1,3,4-Thiadiazol-2-aMine, 5-(2-chlorophenyl)-
5-(2-CHLORO-PHENYL)-[1,3,4]THIADIAZOL-2-YLAMINE
[Molecular Formula]

C8H6ClN3S
[MDL Number]

MFCD00548482
[MOL File]

828-81-9.mol
[Molecular Weight]

211.67
Chemical PropertiesBack Directory
[Melting point ]

192-195 °C
[Boiling point ]

393.8±44.0 °C(Predicted)
[density ]

1.461±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

solid
[pka]

2.28±0.10(Predicted)
[Appearance]

Light yellow to brown Solid
[InChI]

1S/C8H6ClN3S/c9-6-4-2-1-3-5(6)7-11-12-8(10)13-7/h1-4H,(H2,10,12)
[InChIKey]

JKSGNHRIXMYPIO-UHFFFAOYSA-N
[SMILES]

Nc1nnc(s1)-c2ccccc2Cl
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362+P364-P403+P233-P501c
[Hazard Codes ]

Xi,T
[Risk Statements ]

25
[Safety Statements ]

45
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-5-(2-CHLOROPHENYL)-1,3,4-THIADIAZOLE(828-81-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

thiosemicarbazide

79-19-6

2-Chlorobenzoic acid

118-91-2

2-AMINO-5-(2-CHLOROPHENYL)-1,3,4-THIADIAZOLE

828-81-9

5.1.1 Synthesis of 5-(2-chlorophenyl)-1,3,4-thiadiazol-2-amine (68): 2-chlorobenzoic acid (5.18 g, 25 mmol) and aminothiourea (2.28 g, 25 mmol) were dissolved in POCl3 (7 ml) and stirred vigorously for 0.5 hr at 75 °C. After completion of the reaction, H2O (30 ml) was added and the mixture was heated to reflux for 4 hours. Subsequently, the reaction mixture was adjusted with 50% NaOH solution to pH 8. The precipitate was collected by filtration and the filter cake was purified by recrystallization from ethanol to give the yellow crystalline product 68 in a yield of 3.90 g, 88% yield, melting point 190-192 °C (EtOH). The product was analyzed by ESI-MS, m/z: 212.1 [M + H]+; 1H NMR (CDCl3) δ 7.45-7.50 (m, 4H), 7.60-7.62 (m, 1H), 7.99-8.01 (m, 1H). Compounds 60-81 were synthesized in the same way.

[References]

[1] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1999, vol. 38, # 8, p. 998 - 1001
[2] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 21, p. 5766 - 5775
[3] Medicinal Chemistry Research, 2018, vol. 27, # 7, p. 1800 - 1821
[4] Medicinal Chemistry Research, 2012, vol. 21, # 6, p. 816 - 824
[5] Journal of Chemical Research, 2014, vol. 38, # 6, p. 347 - 350
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