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4-Benzothiazolamine,2,5-dimethyl-(9CI) is a yellow, crystalline chemical compound belonging to the benzothiazoles class. It is recognized for its diverse pharmacological properties, such as antibacterial, antifungal, and anti-inflammatory activities, and serves as a valuable intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. Its unique structure and properties establish it as a significant compound in medicinal and organic chemistry.

650635-67-9

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650635-67-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Benzothiazolamine,2,5-dimethyl-(9CI) is used as an intermediate in the synthesis of various drugs and biologically active molecules, contributing to the development of new pharmaceuticals with potential therapeutic applications.
Used in Dye Industry:
4-Benzothiazolamine,2,5-dimethyl-(9CI) is utilized in the production of dyes, where its chemical properties contribute to the creation of a range of colorants for different applications.
Used in Organic Compounds Synthesis:
4-Benzothiazolamine,2,5-dimethyl-(9CI) is employed as a key component in the synthesis of other organic compounds, expanding its utility across various chemical and industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 650635-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,0,6,3 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 650635-67:
(8*6)+(7*5)+(6*0)+(5*6)+(4*3)+(3*5)+(2*6)+(1*7)=159
159 % 10 = 9
So 650635-67-9 is a valid CAS Registry Number.

650635-67-9Relevant academic research and scientific papers

INHIBITORS OF 11-BETA-HYDROXY STEROID DEHYDROGENASE TYPE 1 AND TYPE 2

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Page/Page column 103, (2010/02/06)

There is provided a compound having Formula (I): wherein one of R1 and R2 is a group of the Formula (a), wherein R4 is selected from H and hydrocarbyl, R5 is a hydrocarbyl group and L is an optional linker group, or R1 and R2 together form a ring substituted with the group (Formula (a)) wherein R3 is H or a substituent, and wherein X is selected from S, O, NR6 and C(R7)(R8), wherein R6 is selected from H and hydrocarbyl groups, wherein each of R7 and R8 are independently selected from H and hydrocarbyl groups.

Synthesis and antifungal activity of 6-arylthio-/6-arylamino-4,7-dioxobenzothiazoles

Ryu, Chung-Kyu,Choi, Ko Un,Shim, Ju-Yeon,You, Hea-Jung,Choi, Ik Hwa,Chae, Mi Jin

, p. 4003 - 4008 (2007/10/03)

6-Arylthio-/6-arylamino-4,7-dioxobenzothiazoles were synthesized and tested for in vitro antifungal activity against Candida species and Aspergillus niger. 6-Arylamino-4,7-dioxobenzothiazoles 5 and 6 showed, in general, more potent antifungal activity than 6-arylthio-4,7-dioxobenzothiazoles 3 and 4. The 6-arylamino-substituted compounds 5 and 6 exhibited the greatest activity. In contrast, 6-arylthio-, 2-/5-methyl- or 5-methoxy-moieties of compounds 3-4 did not improve their antifungal activity significantly. The results of this study suggest that 6-arylamino-4,7-dioxobenzothiazoles would be potent antifungal agents.

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