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Benzenecarboximidic acid, N-[(phenylamino)thioxomethyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72149-84-9

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72149-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72149-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,4 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72149-84:
(7*7)+(6*2)+(5*1)+(4*4)+(3*9)+(2*8)+(1*4)=129
129 % 10 = 9
So 72149-84-9 is a valid CAS Registry Number.

72149-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylthiocarbamoyl-benzimidic acid methyl ester

1.2 Other means of identification

Product number -
Other names N-Anilinothioformyl-benziminomethylaether

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:72149-84-9 SDS

72149-84-9Relevant academic research and scientific papers

A simple and efficient approach to the synthesis of 1-phosphonated 5-amino-1-H-[1,2,4]-triazole from N-functionalized imidates

Jabli, Dhiab,Dridi, Khaireddine,Efrit, Mohamed Lotfi

, p. 759 - 764 (2016/05/09)

In this study, we describe a new and easy synthetic approach to variously substituted triazoles based on the reaction of imidates with phosphorylated hydrazine in good yields. A general mechanism of the reactions was also proposed. Characterization of the products was carried out by several analytical and spectroscopic tools including infrared and nuclear magnetic resonance spectroscopies (1H,13C NMR,31P NMR).

One pot synthesis and antimicrobial activity of substituted 2-Aminothiazoles

Al-Ayed, Abdullah Sulaiman

, p. 4081 - 4084 (2015/12/23)

In this work, we described a preparation of substituted 2-Aminothiazoles by two different methods using a one-pot procedure and starting from methoxymethylene-3-Aryl-thiourea (2). The synthesized 2-Aminothiazoles (5a-h) were characterized on the basis of

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