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Carbamic acid, [(1S)-1-(1H-indol-3-ylmethyl)-2-[methyl(phenylmethyl)amino]-2-oxoethyl] -, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

166519-65-9

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166519-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166519-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,5,1 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 166519-65:
(8*1)+(7*6)+(6*6)+(5*5)+(4*1)+(3*9)+(2*6)+(1*5)=159
159 % 10 = 9
So 166519-65-9 is a valid CAS Registry Number.

166519-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-α-tert-butoxycarbonyl-N-benzyl-N-methyltryptophan amide

1.2 Other means of identification

Product number -
Other names [(S)-1-(Benzyl-methyl-carbamoyl)-2-(1H-indol-3-yl)-ethyl]-carbamic acid tert-butyl ester

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:166519-65-9 SDS

166519-65-9Relevant academic research and scientific papers

Novel potent substance P and neurokinin A receptor antagonists. Conception, synthesis and biological evaluation of indolizine derivatives

Millet, Régis,Domarkas, Juozas,Rigo, Benot,Goossens, Laurence,Goossens, Jean-Fran?ois,Houssin, Raymond,Hénichart, Jean-Pierre

, p. 2905 - 2912 (2007/10/03)

Exploration of SAR around dual NK1/NK2 antagonist Cbz-Gly-Leu-Trp-OBzl(CF3)2 and its derivatives disclosed the essential requirements for more potent dual NK1/NK2 binding. We report here the synthesis and the biological properties of a novel series of indolizine including pharmacophoric elements.

L-tryptophan urea amides as NK1/NK2 Dual antagonists

Qi, Hongbo,Shah, Shrenik K.,Cascieri, Margaret A.,Sadowski, Sharon J.,MaCcoss, Malcolm

, p. 2259 - 2262 (2007/10/03)

We report that a systematic modification of an NK1 receptor selective antagonist resulted in the identification of novel compounds, 4c and 4d, with high affinity for both NK1 and NK2 receptors.

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