2-氨基-4-甲基苯并噻唑

小分子

2-氨基-4-甲基苯并噻唑

Z56174289 | A23682 | Tox21_200233 | STK400194 | DTXSID9024487 | NCGC00091579-01 | AS-10773 | DTXCID404487 | FT-0611126 | AS-871/40209246 | NCGC00257787-01 | SCHEMBL94937 | 2-Amino-4-methyl benzothiazole | 2-AMINO-4-METHYLBENZOTHIAZOLE | 4-Methyl-2-aminobe

2-Amino-4-methylbenzothiazole

A119301-500g

500g

≥98%

充氩

常规运输

对湿度敏感

2-Amino-4-methylbenzothiazole is the major degradation product of dufulin pesticide. Adsorption of 2-amino-4-methylbenzothiazole on colloidal silver particles has been investigated by surface enhanced Raman scattering technique. 2-Amino-4-methylbenzothiazole was used in the synthesis of N-(4-methyl-1,3-benzothiazol-yl)-N-[(1,4,5,8-tetramethoxy-2-napthyl)methylidene]amine and Schiff′s base via condensation with 2-acetonaphthone. 2-Amino-4-methylbenzothiazole is the major degradation product of dufulin pesticide. Adsorption of 2-amino-4-methylbenzothiazole on colloidal silver particles has been investigated by surface enhanced Raman scattering technique. 2-Amino-4-methylbenzothiazole was used in the synthesis of N-(4-methyl-1,3-benzothiazol-yl)-N-[(1,4,5,8-tetramethoxy-2-napthyl)methylidene]amine and Schiff′s base via condensation with 2-acetonaphthone.

2-Amino-4-methylbenzothiazole was used in the synthesis of N-(4-methyl-1,3-benzothiazol-yl)-N-[(1,4,5,8-tetramethoxy-2-napthyl)methylidene]amine and Schiff′s base via condensation with 2-acetonaphthone.

1477-42-5

C8H8N2S

164.23 g/mol

129346

216-028-3

MFCD00005793

15132

CC1=C2C(=CC=C1)SC(=N2)N

4-methyl-1,3-benzothiazol-2-amine

1S/C8H8N2S/c1-5-3-2-4-6-7(5)10-8(9)11-6/h2-4H,1H3,(H2,9,10)

GRIATXVEXOFBGO-UHFFFAOYSA-N

CC1=C2C(=CC=C1)SC(=N2)N

488182073

137-139°C

1

3

0

164.041 Da

164.041 Da

67.200 Ų

11

0

151.000

0

1

2.400

129346