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5-methyl-3-(4-nitrophenyl)-1H-1,2,4-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76591-81-6

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76591-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76591-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,9 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76591-81:
(7*7)+(6*6)+(5*5)+(4*9)+(3*1)+(2*8)+(1*1)=166
166 % 10 = 6
So 76591-81-6 is a valid CAS Registry Number.

76591-81-6Relevant academic research and scientific papers

Synthesis and study of novel 1,2,4-triazolylacetic acid derivatives

Khomenko, Dmitro M.,Doroshchuk, Roman O.,Vashchenko, Oleksandr V.,Lampeka, Rostyslav D.

, p. 402 - 408 (2016)

[Figure not available: see fulltext.] A range of 1,2,4-triazolylacetic acids and their derivatives with various substituents at the triazole ring position 3 have been synthesized. The properties of the obtained compounds were studied, showing that: 1) triazolylacetic esters are strong acylating agents; 2) all the obtained triazolylacetic acids underwent decarboxylation when heated to the melting point; 3) the CH2 group in the acetyl moiety can react as methylene component in condensation reactions.

HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES

-

Paragraph 000284, (2016/05/02)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions in need of inhibition of heparan sulfate biosynthesis.

Synthesis of 1,2,4-Triazolines and triazoles utilizing oxazolones

Saleem, Rahman Shah Zaib,Tepe, Jetze J.

experimental part, p. 4330 - 4332 (2010/09/03)

We describe herein a convenient method for the synthesis of 1,2,4-triazolines using oxazolones and azodicarboxylates. Subsequent treatment of these 1,2,4-triazolines with NaOH provides efficient access to the corresponding triazoles.

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