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3-Methyl-2,6-dinitrobenzonitrile is a chemical compound characterized by the molecular formula C8H5N3O4. It is a yellow solid with a molecular weight of 195.14 g/mol. This versatile compound is known for its antimicrobial and pesticidal properties, as well as its role as a potent inhibitor of the enzyme DNA Polymerase β.

948-30-1

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948-30-1 Usage

Uses

Used in Pharmaceutical Industry:
3-Methyl-2,6-dinitrobenzonitrile is used as a starting material for the synthesis of various organic compounds, particularly in the pharmaceutical industry. Its antimicrobial properties make it a valuable intermediate in the production of antimicrobial agents, contributing to the development of new drugs to combat resistant infections.
Used in Agrochemical Industry:
In the agrochemical industry, 3-Methyl-2,6-dinitrobenzonitrile is utilized as a starting material for the synthesis of various organic compounds. Its pesticidal properties are harnessed in the development of pesticides, helping to protect crops from pests and ensure agricultural productivity.
Used in Cancer Research and Drug Development:
3-Methyl-2,6-dinitrobenzonitrile is recognized as a potent inhibitor of the enzyme DNA Polymerase β. This characteristic has significant implications in cancer research, as it can be leveraged in the development of anticancer drugs. By targeting this enzyme, researchers can explore new therapeutic strategies to combat cancer and improve patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 948-30-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 948-30:
(5*9)+(4*4)+(3*8)+(2*3)+(1*0)=91
91 % 10 = 1
So 948-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H5N3O4/c1-5-7(10(12)13)2-6(4-9)3-8(5)11(14)15/h2-3H,1H3

948-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methyl-2,6-dinitrobenzonitrile

1.2 Other means of identification

Product number -
Other names 3,5-Dinitro-4-methyl-benzonitril

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:948-30-1 SDS

948-30-1Relevant academic research and scientific papers

Compound with dual inhibitory activity TDO, IDOO1 and application of compound for treating neurodegenerative disease (by machine translation)

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Paragraph 0083; 0095-0098, (2020/10/06)

The present invention provides a compound of formula I, or a pharmaceutically acceptable salt thereof, or a solvate thereof, which can selectively inhibit TDO, IDOO1, which has a significant inhibitory effect on TDO and/or IDOO1. In addition, the prepared compound has a remarkable anti-tumor effect, has a certain treatment effect on's disease and's disease, and has a good application prospect in the field of medicine preparation. (by machine translation)

Methods of making 6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile and its preferred salt form

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Page 21, (2010/02/08)

6-[(4,5-Dihydro-1H-imidazol-2-yl)amino-]-7-methyl-1H-benzimidazole-4-carbonitrile substantially free of 2,3,7-triamino-4,6-dimethyl-1,9-phenazinedicarbonitrile, and the anhydrous monoacetate salt thereof, are useful in the treatment of alpha-2 mediated di

7-(2-IMIDAZOLINYLAMINO)QUINOLINE COMPOUNDS USEFUL AS ALPHA-2 ADRENOCEPTOR AGONISTS

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, (2008/06/13)

This invention involves involves the use of compounds having the following structure: STR1 wherein: (a) R is unsubstituted C 1-C. sub.3 alkanyl or alkenyl; and(b) R' is selected from hydrogen; unsubstituted C 1-C 3 alkanyl or alkenyl; unsubstituted

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