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193224

Sigma-Aldrich

2-Amino-4-methylbenzothiazole

97%

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About This Item

Formule empirique (notation de Hill):
C8H8N2S
Numéro CAS:
1477-42-5
Poids moléculaire :
164.23
Numéro CE :
216-028-3
Numéro MDL:
MFCD00005793
Code UNSPSC :
12352100
ID de substance PubChem :
24851587
Nomenclature NACRES :
NA.22

Pureté

97%

Pf

137-139 °C (lit.)

Chaîne SMILES 

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)

Clé InChI

GRIATXVEXOFBGO-UHFFFAOYSA-N

Description générale

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.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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2-Methylbenzothiazole 99%

Sigma-Aldrich

112143

2-Methylbenzothiazole

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
Jikang Yoo et al.
Archives of pharmacal research, 31(2), 142-147 (2008-03-28)
A series of nine new compounds bridged by acyl groups at the 5,8-dihydroxyl group of DHNQ were synthesized and their cytotoxic activity against L1210 and P388 cancer cells was examined. Their antitumor action in mice bearing S-180 cells in the
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)
Fabio Gosetti et al.
Environmental science and pollution research international, 22(11), 8288-8295 (2014-12-23)
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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