ChemicalBook--->CAS DataBase List--->20174-68-9

20174-68-9

20174-68-9 Structure

20174-68-9 Structure
IdentificationMore
[Name]

4-Methyl-2-benzothiazolehydrazine
[CAS]

20174-68-9
[Synonyms]

4-METHYL-2-HYDRAZINO BENZOTHIAZOLE
4-methylbenzothiazol-2(3H)-one hydrazone
2-hydrazin-4-methylbenzothiazole
4-METHYL-2(3H)-BENZOTHIAZOLONE YDRAZONE
2(3H)-Benzothiazolone,4-methyl-,hydrazone(9CI)
4-METHYL-2(3H)-BENZOTHIAZOLONEHYDRAZONE
4-Methyl-2-benzothiazolehydrazine
4-METHYL-2(3H)-BENZOTHIAZOLONHYDRAZONE
(4-Methylbenzothiazol-2-yl)hydrazine
4-Methylbenzothiazoline-2-one hydrazone
[EINECS(EC#)]

243-562-4
[Molecular Formula]

C8H9N3S
[MDL Number]

MFCD04448793
[Molecular Weight]

179.242
[MOL File]

20174-68-9.mol
Chemical PropertiesBack Directory
[Melting point ]

167-169 °C
[Boiling point ]

351.5±35.0 °C(Predicted)
[density ]

1.44±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Store in freezer, under -20°C
[pka]

2.62±0.20(Predicted)
[Appearance]

Light brown to yellow Solid
[CAS DataBase Reference]

20174-68-9(CAS DataBase Reference)
[EPA Substance Registry System]

20174-68-9(EPA Substance)
Questions And AnswerBack Directory
[Uses]

2-Hydrazino-4-methylbenzothiazole is used in the synthesis of pesticides.
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2-Amino-4-methylbenzothiazole-->2-Aminobenzothiazole hydrochloride-->Hydrazine monohydrochloride-->Hydrazine hydrate-->Ethylene glycol
[Preparation Products]

Tricyclazole
Safety DataBack Directory
[TSCA ]

TSCA listed
Spectrum DetailBack Directory
[Spectrum Detail]

4-Methyl-2-benzothiazolehydrazine(20174-68-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-4-methylbenzothiazole

1477-42-5

Hydrazine monohydrochloride

2644-70-4

4-Methyl-2-benzothiazolehydrazine

20174-68-9

Example 16: Synthesis of 4-methyl-2-hydrazinylbenzothiazole 4-Methyl-2-aminobenzothiazole (8.21 g, 0.05 mol), hydrazine monohydrochloride (1.14 g, 0.017 mol), 85% hydrazine hydrate (1.96 g, 0.033 mol) and ethylene glycol (41 ml) were mixed under nitrogen protection. The reaction mixture was heated to 140°C and kept at this temperature for 15 hours. Upon completion of the reaction, the mixture was allowed to cool slowly to room temperature and allowed to stand overnight under nitrogen atmosphere. The following morning, water (45 mL) was added to the reaction mixture to promote crystallization. Subsequently, the mixture was filtered and the target product 4-methyl-2-hydrazinylbenzothiazole was isolated. The product was dried under vacuum at 60°C overnight to give a final 8.00 g in 89% yield with a melting point of 143°-151°C. The purity of the product was 85.8% as determined by non-aqueous titration.

[References]

[1] Patent: US3937714, 1976, A
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