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L-Phenylalanine, N,N-bis(carboxymethyl)-, also known as N,N-bis(carboxymethyl)-L-phenylalanine or L-Phenylalanine-N,N-bis(carboxymethyl), is a synthetic amino acid derivative. It is a white crystalline powder with a molecular formula of C12H13NO6 and a molecular weight of 267.23 g/mol. L-Phenylalanine, N,N-bis(carboxymethyl)- is formed by the reaction of L-phenylalanine with two molecules of chloroacetic acid, resulting in the formation of two carboxymethyl groups attached to the nitrogen atom of the amino acid. L-Phenylalanine, N,N-bis(carboxymethyl)- has potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and other bioactive compounds. Its unique structure allows for the formation of stable salts and complexes, making it a valuable building block in the development of new therapeutic agents.

6710-91-4

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6710-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6710-91-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6710-91:
(6*6)+(5*7)+(4*1)+(3*0)+(2*9)+(1*1)=94
94 % 10 = 4
So 6710-91-4 is a valid CAS Registry Number.

6710-91-4SDS

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 (2S)-2-[bis(carboxymethyl)amino]-3-phenylpropanoic acid

1.2 Other means of identification

Product number -
Other names L-Phenylalanine,N,N-bis(carboxymethyl)

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:6710-91-4 SDS

6710-91-4Downstream Products

6710-91-4Relevant academic research and scientific papers

Site-selective recognition of amino acids by Co(III) complexes containing a (N)(O)3-type tripodal tetradentate ligand

Kumita,Morioka,Ozawa,Jitsukawa,Einaga,Masuda

, p. 1035 - 1042 (2007/10/03)

The bis-N,N-carboxymethy-(S)-phenylalaninato carbonato cobalt(III) complex, [Co(bcmpa)(CO3)]2-, has been prepared as a simple model that enables the recognition of an amino acid (Haa) whose coordination behaviours in solution have been characterized by electronic absorption (AB), circular dichroism (CD) and 1H NMR spectroscopies. The reaction of the K2[Co(bcmpa)(CO3)] complex with amino acids (Haa) has predominantly afforded the [Co(bcmpa)(aa)] complex in the trans(N)-configuration mode, rather than in the cis(N)-form. By using amino acid derivatives with bulky substituents at their amino or carboxylate sites under a neutral condition, the reactions have been demonstrated to be initiated by coordination of the amino nitrogen site. Interestingly, the cis(N)-complex, which is isolated as a minor product, isomerizes to the trans(N)-form in the presence of active charcoal under pH 7 in an aqueous solution. The site-selective coordination of Haa to the [Co(bcmpa)(CO3)]2- complex and the stereoselective isomerization of the [Co(bcmpa)(aa)]- complex have been explained to be regulated by weak non-covalent interactions within the ligands, whose origin has been discussed based on a detailed examination of the crystal structures of the trans(N)- and cis(N)-K[Co(bcmpa)(aa)] complexes.

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