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About This Item
Empirical Formula (Hill Notation):
C8H8N2S
CAS Number:
Molecular Weight:
164.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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
Related Categories
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.
Signal Word
Warning
Hazard Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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
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
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Mishra AP and Mishra DP.
International Journal of Pharmacy and Biological Sciences, 2(3), 430-439 (2011)
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This paper reports the study of the photodegradation reactions that tricyclazole can naturally undergo, under the action of sunlight, in aqueous solutions of standard tricyclazole and of the commercial BEAM(TM) formulation. The analyses are carried out by ultra-high performance liquid
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