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N-(p-Chlorophenyl)-p-toluamidine is a chemical compound with the molecular formula C15H13ClN2. It is a derivative of p-toluamidine, which is a compound with potential antimicrobial properties. The addition of a p-chlorophenyl group to the nitrogen atom of p-toluamidine enhances its chemical reactivity and may alter its biological activity. N-(p-Chlorophenyl)-p-toluamidine is often used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to note that the safety and environmental impact of N-(p-Chlorophenyl)-p-toluamidine should be considered, as it contains a chlorine atom which can be a source of concern in terms of environmental persistence and toxicity.

7118-54-9

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7118-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7118-54-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7118-54:
(6*7)+(5*1)+(4*1)+(3*8)+(2*5)+(1*4)=89
89 % 10 = 9
So 7118-54-9 is a valid CAS Registry Number.

7118-54-9SDS

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'-(4-chlorophenyl)-4-methylbenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names N-(4-chloro-phenyl)-4-methyl-benzamidine

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:7118-54-9 SDS

7118-54-9Relevant academic research and scientific papers

Synthesis of 2-arylquinazolin-4(3H)-ones by N-aryl benzamidines with aromatic carbonates

Aikawa, Shunichi,Sekiguchi, Chiharu,Yamazaki, Yuko,Hattori, Mika,Isaka, Tatsuya,Yoshida, Yasuhiko,Ihara, Shogo

, p. 343 - 348 (2014)

The reaction of N-aryl benzamidines 1a, 1b, 1c, 1d, 1e, 1f, 1g, 1h, 1i, 1j, 1k, 1l, 1m, 1n with diphenyl carbonate 2a or ethyl phenyl carbonate 2b synthesized 2-arylquinazolin-4(3H)-ones 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, 3k, 3l, 3m, 3n in simple and

2,3-Diaryl-5-anilino[1,2,4]thiadiazoles as melanocortin MC4 receptor agonists and their effects on feeding behavior in rats

Pan, Kevin,Scott, Malcolm K.,Lee, Daniel H. S.,Fitzpatrick, Louis J.,Crooke, Jeffery J.,Rivero, Ralph A.,Rosenthal, Daniel I.,Vaidya, Anil H.,Zhao, Boyu,Reitz, Allen B.

, p. 185 - 192 (2007/10/03)

The melanocortin-4 receptor (MC4) modulates physiological functions such as feeding behavior, nerve regeneration, and drug addiction. Using a high throughput screen based on 125I-NDP-MSH binding to the human MC4 receptor, we discovered 2,3-diar

Reactions of Aryliminodimagnesium with Some N,N-Dimethylcarboxamides and Benzonitriles Affording Various Types of Amidines. Correction of Previous Results on Formamidine Formation from N,N-Dimethylformamide

Okubo, Masao,Tanaka, Mikio,Murata, Yuri,Tsurusaki, Nobuyuki,Omote, Yasumasa,et al.

, p. 1965 - 1968 (2007/10/02)

Some symmetrical and unsymmetrical form- and benzamidines were prepared by the reaction of ArN(MgBr)2 with Ar'CN, HCONMe2 and related compounds in tetrahydrofuran.

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