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About This Item
Empirical Formula (Hill Notation):
C8H8N2S
CAS Number:
Molecular Weight:
164.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
216-028-3
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
137-139 °C (lit.)
SMILES string
Cc1cccc2sc(N)nc12
InChI
1S/C8H8N2S/c1-5-3-2-4-6-7(5)10-8(9)11-6/h2-4H,1H3,(H2,9,10)
InChI key
GRIATXVEXOFBGO-UHFFFAOYSA-N
General description
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.
Application
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.
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Jyotirmoy Sarkar et al.
The journal of physical chemistry. B, 109(47), 22536-22544 (2006-07-21)
The adsorption of 2-amino-4-methylbenzothiazole (2-AMBT) on colloidal silver particles has been investigated by a surface enhanced Raman scattering (SERS) study. The SERS spectra of the 2-AMBT molecule at varied adsorbate concentrations recorded in different time domains are compared with its
Hua Zi Wang et al.
Environmental science and pollution research international, 21(6), 4331-4342 (2013-12-11)
Dufulin is a newly developed antiviral agent (or pesticide) that activates systemic acquired resistance of plants. This pesticide is widely used in China to prevent abroad viral diseases in rice, tobacco and vegetables. In this study, the potential impacts such
SYNTHESIS, STRUCTURAL CHARACTERIZATION AND ANTIMICROBIAL ACTIVITIES OF SOME TRANSITION METAL COMPLEXES CONTAINING 2-ACETONAPHTHONE.
Mishra AP and Mishra DP.
International Journal of Pharmacy and Biological Sciences, 2(3), 430-439 (2011)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 193224-25G | 04061838760708 |
