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Benzaldehyde, 4-nitro-, (diphenylmethylene)hydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60766-79-2

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60766-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60766-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,6 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60766-79:
(7*6)+(6*0)+(5*7)+(4*6)+(3*6)+(2*7)+(1*9)=142
142 % 10 = 2
So 60766-79-2 is a valid CAS Registry Number.

60766-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitrobenzaldehyde N-(diphenylmethylene)hydrazone

1.2 Other means of identification

Product number -
Other names N-Benzhydrylidene-N'-[1-(4-nitro-phenyl)-meth-(E)-ylidene]-hydrazine

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:60766-79-2 SDS

60766-79-2Downstream Products

60766-79-2Relevant academic research and scientific papers

Anti-cancer potential of benzophenone-bis-Schiff bases on human pancreatic cancer cell line

Khan, Khalid Mohammed,Rasheed, Huma,Fatima, Bibi,Hayat, Muhammad,Rahim, Fazal,Ullah, Hayat,Hameed, Abdul,Taha, Muhammad,Tahir, Affan,Perveen, Shahnaz

, p. 954 - 958 (2016/11/22)

Synthetic benzophenone-bis-Schiff bases (1-17) were evaluated for PC3 cell line inhibition. Most of the compounds showed cytotoxic effects but compounds 4, 8, 14, 16, and 17 were found to be potent. The growth inhibition of PC3 cells was in a concentratio

Synthesis of benzophenone hydrazone analogs and their DPPH radical scavenging and urease inhibitory activities

Khan, Khalid Mohammed,Rahim, Fazal,Khan, Ajmal,Ali, Sajjad,Taha, Muhammad,Saad, Syed Muhammad,Khan, Momin,Najeebullah,Shaikh,Perveen, Shahnaz,Choudhary, Muhammad Iqbal

, p. 479 - 483 (2015/08/04)

Benzophenone hydrazone analogs 1-25 were synthesized and evaluated for antioxidant (DPPH radical scavenging), and urease inhibitory activities. Out of twenty-five analogs, compounds 8, 23, and 1 showed potent free radical scavenging activities with ICsub

Synthesis of benzophenonehydrazone schiff bases and their in vitro antiglycating activities

Khan, Khalid Mohammed,Rahim, Fazal,Ambreen, Nida,Taha, Muhammad,Khan, Momin,Jahan, Humaira,Najeebullah,Shaikh, Azizuddin,Iqbal, Sarosh,Perveen, Shahnaz,Choudhary, Muhammad Iqbal

, p. 588 - 595 (2013/07/28)

Benzophenonehydrazone Schiff bases 1-25 were synthesized and their in vitro antiglycation potential has been studied. Out of twenty-five compounds, thirteen showed varying degrees of antiglycation activity with IC50 values ranging between 25.7

An expeditious and solvent free synthesis of azine derivatives using sulfated anatase-titania as a novel solid acid catalyst

Krishnakumar,Swaminathan

experimental part, p. 50 - 55 (2012/02/04)

Solid acid catalyst sulfated anatase-titania (TiO2-SO 42-) has been used for the synthesis of azine derivatives from benzophenone hydrazone and ketones/aldehydes by simple physical grinding. This sulfated titania gives an

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