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D-Phe-L-Val-OH, also known as D-Phenylalanine-L-Valine-OH, is a tripeptide consisting of two amino acids, D-Phenylalanine and L-Valine, connected by a peptide bond. D-Phenylalanine is an essential amino acid, while L-Valine is a branched-chain amino acid. This specific combination of amino acids is not commonly found in proteins, making it a unique compound. D-Phe-L-Val-OH has potential applications in pharmaceutical research, particularly in the development of novel therapeutic agents, as well as in the study of peptide synthesis and structure. Its properties, such as solubility and stability, can be investigated for various biotechnological and medicinal purposes.

3496-45-5

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3496-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3496-45-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3496-45:
(6*3)+(5*4)+(4*9)+(3*6)+(2*4)+(1*5)=105
105 % 10 = 5
So 3496-45-5 is a valid CAS Registry Number.

3496-45-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-Phe-(S)-Val-OH

1.2 Other means of identification

Product number -
Other names (S)-2-((R)-2-Amino-3-phenyl-propionylamino)-3-methyl-butyric acid

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:3496-45-5 SDS

3496-45-5Downstream Products

3496-45-5Relevant academic research and scientific papers

NEW APPROACHES TO THE ASYMMETRIC SYNTHESIS OF NON-PROTEINOGENIC α-AMINO ACIDS AND DIPEPTIDES THROUGH CHIRAL β-LACTAM INTERMEDIATES

Ojima, Iwao,Chen, Hauh-Jyun C.,Qiu, Xiaogang

, p. 5307 - 5318 (2007/10/02)

Novel and effective routes to optically pute aromatic α-amino acids, α-methyl-α-amino acids and their derivatives including dipeptides are developed via homochiral β-lactams which are obtained through asymmetric cycloadditions of ketenes to imines.

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