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

17922-76-8

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17922-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17922-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,2 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17922-76:
(7*1)+(6*7)+(5*9)+(4*2)+(3*2)+(2*7)+(1*6)=128
128 % 10 = 8
So 17922-76-8 is a valid CAS Registry Number.

17922-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-Cyclohexylcarbamoyl-ethyl)-carbamic acid benzyl ester

1.2 Other means of identification

Product number -
Other names -

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:17922-76-8 SDS

17922-76-8Relevant academic research and scientific papers

Synthesis, characterization and docking studies of anti-HCV molecules

Kumar, Satish,Santra,Dwivedi,Aryan

, p. 1221 - 1229 (2020/06/09)

The present study reports the synthesis and characterization of novel molecules inhibiting the spread of hepatitis C. The molecules were designed as to block the NS3/4A protease enzyme on HCV RNA. The molecules were synthesized using usual peptide synthesis techniques. Compounds with purity more than 95% were characterized and docking studies were also performed. All the compounds were characterized using physico-chemical techniques such as determination of melting point by DSC and NMR, mass, IR spectral studies. The docking studies were also conducted to assess the activity of molecules for inhibition of hepatitis C virus.

Stereoselectivity and regioselectivity in nucleophilic ring opening in derivatives of 3-phenylisoxazolo[2,3-a]pyrimidine. Unpredicted dimerization and ring transformation. Syntheses of derivatives of pyrimidinylmethylamine, pyrimidinylmethylamino acid ami

Zvilichovsky, Gury,Gbara-Haj-Yahia, Isra

, p. 4966 - 4973 (2007/10/03)

The nucleophilic ring opening of the isoxazolone ring in 2-oxo-3-phenylisoxazolo[2,3-a]pyrimidine derivatives by optically active amino acid amides and ephedrine led to pyrimidinylmethylamino acid amides. Using amides of different L-amino acids and (-)-ep

Synthesis of Polyamine Analoa of Spider Toxins

Benz, Herbert,Hesse, Manfred

, p. 957 - 971 (2007/10/02)

Within the last few years, polyamine toxins derived from various arthropods raised increasing interest due their interaction with glutamate receptors of insects and invertebrates.Compounds 51 and 52 were prepared together with 53-58 to study a new pathway

DIPEPTIDE DERIVATIVES

-

, (2008/06/13)

The present disclosure relates to dipeptide derivatives. These novel compounds are useful as elastase inhibitors.

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