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nicotinic acid N2-(3,4,5-trimethoxybenzylidene)hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

201015-36-3

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201015-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201015-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,0,1 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 201015-36:
(8*2)+(7*0)+(6*1)+(5*0)+(4*1)+(3*5)+(2*3)+(1*6)=53
53 % 10 = 3
So 201015-36-3 is a valid CAS Registry Number.

201015-36-3Downstream Products

201015-36-3Relevant academic research and scientific papers

Investigation of nicotinamide and isonicotinamide derivatives: A quantitative and qualitative structural analysis

Purushothaman, Gayathri,Angira, Deekshi,Thiruvenkatam

, p. 34 - 44 (2019)

An anhydrous nature of benzylidene derivatives of nicotin and isonicotinamides crystal structures is determined and studied for their weak intermolecular interactions. The molecular structure is non-planar in general with the pyridine ring twisted with re

Nicotinic acid benzylidene/phenyl-ethylidene hydrazides: Synthesis, antimicrobial evaluation and QSAR studies

Narang, Rakesh,Narasimhan, Balasubramanian,Sharma, Sunil,Sriram, Dharmarajan,Yogeeswari, Perumal,De Clercq, Erik,Pannecouque, Christophe,Balzarini, Jan

, p. 733 - 749 (2012/05/05)

A series of nicotinic acid hydrazides (1-19) was synthesized and tested in vitro for antimycobacterial, antiviral, antibacterial and antifungal activities. The antimycobacterial activity results indicated that the presence of electron withdrawing halo groups improved the antimycobacterial activity. The antiviral evaluation showed that none of the synthesized derivatives inhibited the replication of viruses at subtoxic concentrations, except compounds 9 and 12. The antimicrobial screening results demonstrated that compounds having methoxy and 2-hydroxy naphthalene substituents were the most active ones against tested microbial strains. QSAR investigations revealed that multi-target QSAR models were found to be more effective in describing the antimicrobial activity than one-target QSAR models.

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