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3-Methyl-1,2,4-triazol-5-one is a synthetic chemical compound belonging to the triazolone class, characterized by a triazole ring with a methyl group at the 3-position. It is recognized for its versatile nature and serves as an important intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals.

930-63-2

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930-63-2 Usage

Uses

Used in Pharmaceutical Industry:
3-Methyl-1,2,4-triazol-5-one is used as a key intermediate for the synthesis of various pharmaceuticals due to its biological activities, which include anti-inflammatory and antifungal properties. Its molecular structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Methyl-1,2,4-triazol-5-one is utilized as a building block for the creation of herbicidal compounds. Its herbicidal properties make it a valuable component in the production of agricultural chemicals aimed at controlling weed growth, thereby enhancing crop yields.
Used in Organic Synthesis:
3-Methyl-1,2,4-triazol-5-one is employed as a versatile intermediate in organic synthesis, facilitating the construction of complex organic molecules for a wide range of applications in medicinal and agricultural chemistry. Its unique structure and reactivity contribute to the development of innovative chemical entities with diverse functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 930-63-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 930-63:
(5*9)+(4*3)+(3*0)+(2*6)+(1*3)=72
72 % 10 = 2
So 930-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H5N3O/c1-2-4-3(7)6-5-2/h1H3,(H2,4,5,6,7)

930-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-1,2-dihydro-1,2,4-triazol-3-one

1.2 Other means of identification

Product number -
Other names 4,5-dihydro-3-methyl-5-oxo-1H-1,2,4-triazole

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:930-63-2 SDS

930-63-2Relevant academic research and scientific papers

Non-Nucleoside reverse transcriptase inhibitors

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Page/Page column 15, (2009/01/23)

Compounds of formula I, wherein R1, R2, R3, X and Ar, are as defined herein or pharmaceutically acceptable salts thereof, inhibit HIV-1 reverse transcriptase and afford a method for prevention and treatment of HIV-1 infections and the treatment of AIDS and/or ARC. The present invention also relates to compositions containing compounds of formula I useful for the prevention and treatment of HIV-1 infections and the treatment of AIDS and/or ARC.

DISILYLATED COMPOUNDS AS PRECURSORS OF HETEROCYCLES: SYNTHESIS OF BENZIMIDAZOLES, TRIAZOLES, FURAN AND PYRROLE.

Rigo, Benoit,Valligny, Dominique,Taisne, Sophie

, p. 167 - 180 (2007/10/02)

The cyclization of disilylated compounds catalyzed by trifluoromethanesulfonoc acid is an easy way to obtain some heterocycles such as benzimidazole, triazole, furan and pyrrole.

ACETALS OF LACTAMS AND ACID AMIDES. 37. * REACTIONS OF AMIDE AND LACTAM ACETALS WITH DERIVATIVES OF UREA AND URETHANE AND SYNTHESIS OF CONDENSED PYRIMIDINES

Kaimanakova, S. I.,Kuleshova, E. F.,Solov'eva, N. P.,Granik, V. G.

, p. 1208 - 1211 (2007/10/02)

The reactions of diethylacetals of dimethylacetamide and N-methylbutyro-, -valero-, and -caprolactams with urea, thiourea, and urethane lead to the corresponding N-carbamide- and N-ethoxycarbonylamides, on the basis of which derivatives of pyrimidine and pyrrolo- and pyridopyrimidine and pyridoazepine, as well as triazole derivatives, were synthetized.

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