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50871-65-3

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50871-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50871-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,7 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50871-65:
(7*5)+(6*0)+(5*8)+(4*7)+(3*1)+(2*6)+(1*5)=123
123 % 10 = 3
So 50871-65-3 is a valid CAS Registry Number.

50871-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-naphthalen-2-ylbenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names Benzenecarboximidamide,N-2-naphthalenyl

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:50871-65-3 SDS

50871-65-3Relevant articles and documents

ORGANIC ELECTROLUMINESCENT MATERIAL AND DEVICE

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Paragraph 0158; 0159; 0160; 0161, (2021/05/07)

A compound having a first ligand of the following is described. Ring A represents a monocyclic aromatic group or a polycyclic aromatic group. Ring B represents a polycyclic aromatic group. Z is a carbon. Z and the right N are coordinated to a metal to form a five-membered chelate ring. R1 and R2 independently represent mono to a maximum possible number of substitutions, or no substitution.

Acid-catalyzed synthesis of imidazole derivatives via N-phenylbenzimidamides and sulfoxonium ylides cyclization

Tian, Yuan,Qin, Mingda,Yang, Xueying,Zhang, Xueguo,Liu, Yafeng,Guo, Xin,Chen, Baohua

supporting information, p. 2817 - 2823 (2019/04/13)

A straightforward method to synthesize imidazole derivatives from amidines and sulfoxonium ylides catalyzed by acids is reported in this study. Specifically, catalyzed by trifluoroacetic acid in DCE solvents can improve synthesis efficiency under metal-fr

Ligand-free copper-catalyzed arylation of amidines

Cortes-Salva, Michelle,Garvin, Corey,Antilla, Jon C.

supporting information; experimental part, p. 1456 - 1459 (2011/04/26)

Copper-catalyzed cross-coupling reactions of amidine salts were utilized to synthesize monoarylated amidines in moderate to high yields with ligand-free conditions. DMF was the superior solvent for the N-arylation of benzamidines, while MeCN was used in the formation of N-aryl amidines in moderate to high yield.(Figure Presented)

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