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L-Phenylalanine, an essential amino acid, and N-D-phenylalanyl-, a peptide bond formed between two phenylalanine molecules, are both crucial components in various biological processes. L-Phenylalanine is a building block for proteins and plays a vital role in the synthesis of neurotransmitters, such as dopamine and norepinephrine. It is also involved in the production of melanin, a pigment responsible for skin, hair, and eye color. N-D-phenylalanyl-, on the other hand, represents a dipeptide formed by the condensation of two phenylalanine molecules, with the removal of a water molecule. This peptide bond is essential for the formation of larger polypeptide chains and proteins, which are vital for various cellular functions and structural components. Both L-Phenylalanine and N-D-phenylalanyl- contribute significantly to the maintenance of overall health and the proper functioning of the human body.

2577-22-2

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2577-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2577-22-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,7 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2577-22:
(6*2)+(5*5)+(4*7)+(3*7)+(2*2)+(1*2)=92
92 % 10 = 2
So 2577-22-2 is a valid CAS Registry Number.

2577-22-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[[(2R)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoic acid

1.2 Other means of identification

Product number -
Other names L-Phenylalanine,N-D-phenylalanyl

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:2577-22-2 SDS

2577-22-2Downstream Products

2577-22-2Relevant 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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