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Benzoic acid, 4-methoxy-, 2-benzoyl-1-phenylhydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41214-60-2

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41214-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41214-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41214-60:
(7*4)+(6*1)+(5*2)+(4*1)+(3*4)+(2*6)+(1*0)=72
72 % 10 = 2
So 41214-60-2 is a valid CAS Registry Number.

41214-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-benzoyl-4-methoxy-N-phenylbenzohydrazide

1.2 Other means of identification

Product number -
Other names -

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:41214-60-2 SDS

41214-60-2Downstream Products

41214-60-2Relevant academic research and scientific papers

Ligand-free Cu(ii)-mediated aerobic oxidations of aldehyde hydrazones leading to N,N′-diacylhydrazines and 1,3,4-oxadiazoles

Liu, Lei,Feng, Suliu

, p. 2585 - 2592 (2017)

A Cu(ii)-mediated synthesis of N,N′-diacylhydrazines and 1,3,4-oxadiazoles from aldehyde hydrazones has been developed. This is the first time that the synthesis of N,N′-diacylhydrazines and 1,3,4-oxadiazoles using N,N-dimethylamides as the acylation reagent and O2 in air as the oxidation reagent is reported. These reactions offered several advantages including simple workups, ligand-free inexpensive metal salts as mediators, high yields, and wide scope of substrates.

The Reaction of 1-(N-Phenacylidene)amino-1,2,3-triazoles with Diphenylnitrilimine

Bojilova, A.,Rodios, N. A.,Tsoleridis, C. A.,Alexandrou, N. E.

, p. 735 - 738 (2007/10/02)

Diphenylnitrilimine reacts with 1-(N-phenacylidene)amino-1,2,3-triazoles 1 to give mainly 1,2,4- and 2H-1,2,3-triazoles 2 and 3.CNDO/2 calculations were made on the compounds 1 and the cycloaddition was also examined on the basis of the interacting fronti

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