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Benzothiazole, 2,5-dimethyl-4-nitro(9CI) is a chemical compound characterized by the molecular formula C9H8N2O2S. It is a nitro derivative of benzothiazole, featuring a unique structure with both a nitro group and two methyl groups attached to the benzothiazole ring. Benzothiazole, 2,5-dimethyl-4-nitro(9CI) is known for its distinctive properties and is commonly utilized in the production of dyes, pesticides, and pharmaceuticals. Due to its potential hazards, it should be handled with care by trained professionals in controlled laboratory settings.

650635-66-8

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650635-66-8 Usage

Uses

Used in Dye Industry:
Benzothiazole, 2,5-dimethyl-4-nitro(9CI) is used as a chemical intermediate for the synthesis of various dyes. Its unique structure contributes to the color and stability of the dyes produced, making it a valuable component in this industry.
Used in Pesticide Industry:
In the pesticide industry, Benzothiazole, 2,5-dimethyl-4-nitro(9CI) serves as a key ingredient in the formulation of certain pesticides. Its chemical properties allow it to effectively target and control pests, contributing to improved crop protection and yield.
Used in Pharmaceutical Industry:
Benzothiazole, 2,5-dimethyl-4-nitro(9CI) is utilized as a building block in the development of pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the creation of new drugs with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 650635-66-8 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 650635-66:
(8*6)+(7*5)+(6*0)+(5*6)+(4*3)+(3*5)+(2*6)+(1*6)=158
158 % 10 = 8
So 650635-66-8 is a valid CAS Registry Number.

650635-66-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethyl-4-nitro-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names Benzothiazole,2,5-dimethyl-4-nitro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:650635-66-8 SDS

650635-66-8Upstream product

650635-66-8Relevant academic research and scientific papers

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 (2003)

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.

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.

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