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Naphthalen-1-yl-acetic acid benzylidenehydrazide is a complex organic compound with the chemical formula C20H17N3O. It is derived from naphthalene, a polycyclic aromatic hydrocarbon, and features a benzylidene group attached to a hydrazide moiety. naphthalen-1-yl-acetic acid benzylidenehydrazide is characterized by its white crystalline appearance and is soluble in various organic solvents. It is synthesized through a condensation reaction between naphthalen-1-yl-acetic acid and benzylidenehydrazine, and is used in the pharmaceutical industry as an intermediate for the synthesis of various drugs, particularly those with anti-inflammatory and analgesic properties. Due to its potential applications in medicine, research on naphthalen-1-yl-acetic acid benzylidenehydrazide focuses on its chemical properties, stability, and pharmacological effects.

1094-37-7

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1094-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1094-37-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1094-37:
(6*1)+(5*0)+(4*9)+(3*4)+(2*3)+(1*7)=67
67 % 10 = 7
So 1094-37-7 is a valid CAS Registry Number.

1094-37-7Downstream Products

1094-37-7Relevant academic research and scientific papers

Substituted naphthalen-1-yl-acetic acid hydrazides: Synthesis, antimicrobial evaluation and QSAR analysis

Narang, Rakesh,Narasimhan, Balasubramanian,Sharma, Sunil,De Clercq, Erik,Pannecouque, Christophe,Balzarini, Jan

, p. 249 - 274 (2013/07/28)

A series of naphthalen-1-yl-acetic acid benzylidene/(1-phenyl-ethylidene)- hydrazides (1-36) was synthesized and tested, in vitro, for antiviral, antibacterial and antifungal activities. The antibacterial and antifungal screening results indicated that compounds having o-bromo, methoxy and hydroxy substitutents were the most active ones. The results of antiviral evaluation showed that none of the synthesized derivatives inhibited the viral infection at subtoxic concentrations. QSAR investigations revealed that the multi-target QSAR model was more effective in describing the antimicrobial activity than the one-target QSAR models. Further, it revealed the importance of the partition coefficient (log P) followed by energies of the highest occupied molecular orbital (HOMO) and topological parameters, molecular connectivity indices ( 1X, 3X and 3Xv) in describing the antimicrobial activity of substituted hydrazides.

An expedient method for the synthesis of acylhydrazones under microwave irradiation in solvent-free medium

Li, Jian-Ping,Zheng, Peng-Zhi,Zhu, Jun-Ge,Liu, Rui-Jie,Qu, Gui-Rong

, p. 90 - 92 (2007/10/03)

A simple, efficient and eco-friendly method for the synthesis of acylhydrazones from acylhydrazides and aldehydes under microwave (MW) irradiation was reported, no solvent and catalyst was used. The method is combined with a combinatorial approach and fou

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