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Benzoic acid, 2-acetyl-2-methylhydrazide is a chemical compound with the molecular formula C10H12N2O2. It is a derivative of benzoic acid, where the carboxylic acid group is replaced by a 2-acetyl-2-methylhydrazide group. Benzoic acid,2-acetyl-2-methylhydrazide is an organic compound that belongs to the class of hydrazides, which are characterized by the presence of a hydrazine group (-NH-NH2) bonded to a carbonyl group. Benzoic acid, 2-acetyl-2-methylhydrazide is a white crystalline solid and is used in various chemical reactions and as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Its chemical structure and properties make it a versatile building block in organic synthesis, particularly in the preparation of complex molecules with potential applications in the fields of medicine and materials science.

6327-62-4

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6327-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6327-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6327-62:
(6*6)+(5*3)+(4*2)+(3*7)+(2*6)+(1*2)=94
94 % 10 = 4
So 6327-62-4 is a valid CAS Registry Number.

6327-62-4Downstream Products

6327-62-4Relevant academic research and scientific papers

Evidence of an nN(amide) → π*ArInteraction in N-Alkyl- N, N′-diacylhydrazines

Deka, Jugal Kishore Rai,Sahariah, Biswajit,Sakpal, Sushil S.,Bar, Arun Kumar,Bagchi, Sayan,Sarma, Bani Kanta

, p. 7003 - 7007 (2021/05/26)

1,2-Dibenzoyl-1-tert-butylhydrazine (RH-5849) and related N-alkyl-N,N′-diacylhydrazines are environmentally benign insect growth regulators. Herein, we show that an unusual nN(amide) → π*Ar interaction mediated by a hydrazide amide nitrogen atom plays a crucial role in stabilizing their biologically active trans-cis (t-c) rotameric conformations. We provide NMR and IR spectroscopic evidence for the presence of these interactions, which is also supported by X-ray crystallographic and computational studies.

Conformational control ofN-methyl-N,N'-diacylhydrazines by noncovalent carbon bonding in solution

Bar, Arun Kumar,Baruah, Kalpita,Deka, Jugal Kishore Rai,Sahariah, Biswajit,Sarma, Bani Kanta

, p. 4874 - 4877 (2020/05/13)

In recent years, some X-ray structural and computational evidence has emerged for noncovalent carbon bonding (C-bond). However, evidence of C-bonds in solution is limited. Herein, from the conformational analyses of strategically designedN-methyl-N,N'-dia

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