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Phenylalanine, N-[(4-chlorophenyl)methylene]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100992-42-5

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100992-42-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100992-42-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,9 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100992-42:
(8*1)+(7*0)+(6*0)+(5*9)+(4*9)+(3*2)+(2*4)+(1*2)=105
105 % 10 = 5
So 100992-42-5 is a valid CAS Registry Number.

100992-42-5SDS

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 (RS)-N-(4-chlorobenzylidene)phenylalanine methyl ester

1.2 Other means of identification

Product number -
Other names 2-{[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-amino}-3-phenyl-propionic acid methyl 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:100992-42-5 SDS

100992-42-5Relevant academic research and scientific papers

Complete deracemization by attrition-enhanced Ostwald ripening elucidated

Noorduin, Wim L.,Meekes, Hugo,Van Enckevort, Willem J. P.,Millemaggi, Alessia,Leeman, Michel,Kaptein, Bernard,Kellogg, Richard M.,Vlieg, Elias

supporting information; experimental part, p. 6445 - 6447 (2009/03/11)

(Chemical Equation Presented) Shaken and stirred: The emergence of single chirality in the solid state during grinding of a slurry has been kinetically studied for a phenylglycine amide (see scheme). The insight obtained into the underlying process of attrition-enhanced Ostwald ripening enables the definition of suitable conditions to increase the deracemization rate drastically.

Amide Bond Replacements: Incorporation of a 2,5,5-Trisubstituted Imidazoline into Dipeptides and into a CCK-4 Derivative.

Gilbert, Ian,Rees, David C.,Richardson, Reginald S.

, p. 2277 - 2280 (2007/10/02)

Synthetic methodology for the introduction of a 2,5,5-trisubstituted imidazoline ring as an amide replacement into dipeptide derivatives of Phe, Trp, Lys(N6-CBZ) and Nle is described.This replacement is also incorporated into the Trp-Nle bond o

N-SUBSTITUTED AMINO ACID DERIVATIVES WITH HYPERALPHALIPOPROTEINAEMIC ACTIVITY

Baggaley, Keith H.,Fears, Robin,Ferres, Harry,Geen, Graham R.,Hatton, Ian K.,et al.

, p. 523 - 532 (2007/10/02)

A series of N-substituted amino acid derivatives was synthesized and the compounds were evaluated for their effects on serum total cholesterol, HDL cholesterol and triglycerides in experimental animals.Hyperalphalipoproteinaemic activity was found for some of these compounds tested, especially BRL 26314 (2) and related 3-aryl-2-aminopropionic acids.Structure-activity relationships are discussed.Keywords: N-substituted amino acid derivatives / hyperalphalipoproteinaemic activity

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