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N-benzyl-N'-(4-chlorophenyl)-N-methylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

203585-29-9

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203585-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203585-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,5,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 203585-29:
(8*2)+(7*0)+(6*3)+(5*5)+(4*8)+(3*5)+(2*2)+(1*9)=119
119 % 10 = 9
So 203585-29-9 is a valid CAS Registry Number.

203585-29-9Downstream Products

203585-29-9Relevant academic research and scientific papers

Novel CRAC channel conditioning agent, and preparation method and applications thereof

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Paragraph 0338; 0339; 0340; 0344, (2016/10/08)

The invention provides a novel CRAC (calcium release-activated calcium) channel conditioning agent, and a preparation method and applications thereof, and more specifically, the invention provides a compound represented by formula I, and the groups are defined in the patent specification. The invention also provides the preparation method of the compound represented by formula I, and applications of the compound as a CRAC channel conditioning agent.

One-pot synthesis of trisubstituted ureas from achloroaldoxime O-methanesulfonates and secondary amines

Kaeobamrung, Juthanat,Lanui, Asan,Mahawong, Sirinad,Duangmak, Witthawin,Rukachaisirikul, Vatcharin

, p. 58587 - 58594 (2018/02/19)

Trisubstituted ureas can be synthesized in a one-pot fashion from bench-stable a-chloroaldoxime Omethanesulfonates and secondary amines under mild reaction conditions. Two practical protocols have been developed to achieve various urea syntheses from both secondary aromatic amines and aliphatic amines.

Novel quenchers for solution phase parallel synthesis

Nikam, Sham S.,Kornberg, Brian E.,Ault-Justus, Stephanie E.,Rafferty, Michael F.

, p. 1121 - 1124 (2007/10/03)

The bifunctionality of amino acids can be exploited by utilizing them as quenchers in rapid solution phase parallel synthesis. The amino group was used to covalently trap the excess electrophiles, whereas the carboxylic acid moiety was used to solubilize

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