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1-methyl-4-nitro-1H-1,2,3-Triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107945-66-4

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107945-66-4 Usage

Molecular structure

A triazole ring with a methyl group at position 1 and a nitro group at position 4.

Functional groups

Nitro group, methyl group.

Triazole family

Member of a family of compounds with a triazole ring structure.

Building block

Used in organic synthesis and pharmaceutical research.

Antimicrobial properties

Potential to inhibit the growth of microorganisms.

Antitumor properties

Potential to inhibit the growth of cancer cells.

Enzyme inhibition

Ability to inhibit certain enzymes, which may have therapeutic applications.

Lead compound

Has shown promise as a potential lead compound for the development of new drugs.

Medicinal chemistry and chemical biology research

Its unique structure and chemical properties make it a valuable tool for these research fields.

Check Digit Verification of cas no

The CAS Registry Mumber 107945-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,4 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107945-66:
(8*1)+(7*0)+(6*7)+(5*9)+(4*4)+(3*5)+(2*6)+(1*6)=144
144 % 10 = 4
So 107945-66-4 is a valid CAS Registry Number.

107945-66-4Relevant academic research and scientific papers

HETEROARYL PYRIDONE AND AZA-PYRIDONE COMPOUNDS AS INHIBITORS OF BTK ACTIVITY

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Paragraph 1182; 1183, (2015/11/16)

Heteroaryl pyridone and aza-pyridone compounds of Formula I are provided, where one or two of X, X, and Xare N, and including stereoisomers, tautomers, and pharmaceutically acceptable salts thereof, useful for inhibiting Btk kinase, and for treating immune disorders such as inflammation mediated by Btk kinase. Methods of using compounds of Formula I foranddiagnosis, and treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

8-FLUOROPHTHALAZIN-1(2H)-ONE COMPOUNDS

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Paragraph 0500, (2013/05/21)

8-Fluorophthalazin-1(2h)-one compounds of Formula II where one or two of X1, X2, and X3 are N, are provided, including stereoisomers, tautomers, and pharmaceutically acceptable salts thereof, useful for inhibiting Btk kinase, and for treating immune disorders such as inflammation mediated by Btk kinase. Methods of using compounds of Formula II for in vitro, in situ, and in vivo diagnosis, and treatment of such disorders in mammalian cells, or associated pathological conditions, are disclosed.

REACTIONS OF 4-NITRO-1,2,3-TRIAZOLE WITH ALKYLATING AGENTS AND COMPOUNDS WITH ACTIVATED MULTIPLE BONDS

Vereshchagin, L. I.,Kuznetsova, N. I.,Kirillova, L. P.,Shcherbakov, V. V.,Sukhanov, G. T.,Gareev, G. A.

, p. 745 - 748 (2007/10/02)

When 4-nitro-1,2,3-triazole is alkylated, a mixture of N1- and N2-isomers is formed, with the latter usually predominating.The same behavior is also observed in addition reactions of 4-nitrotriazole to activated multiple bonds.

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