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L-Phenylalaninamide, D-α-aspartyl- is a synthetic compound that combines the amino acid L-phenylalanine with D-aspartic acid through an amide linkage. L-Phenylalaninamide, D-a-aspartyl- is of interest in the field of medicinal chemistry and may have potential applications in the development of drugs targeting various conditions. The combination of these two amino acids creates a unique molecule with specific properties that can be explored for therapeutic use. The L-phenylalanine component contributes to its aromatic nature, while the D-aspartic acid provides a chiral center and acidic properties. Research into such compounds can lead to a better understanding of their interactions with biological systems and their potential as therapeutic agents.

5241-72-5

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5241-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5241-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,4 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5241-72:
(6*5)+(5*2)+(4*4)+(3*1)+(2*7)+(1*2)=75
75 % 10 = 5
So 5241-72-5 is a valid CAS Registry Number.

5241-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name D-Asp-Phe-NH2

1.2 Other means of identification

Product number -
Other names D-Asp-L-Phe-amide

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:5241-72-5 SDS

5241-72-5Upstream product

5241-72-5Downstream Products

5241-72-5Relevant academic research and scientific papers

Aspartate Racemization in Synthetic Peptides. Part 2. Tendency to Racemization of Aminosuccinyl Residue

Schoen, Istvan,Szirtes, Tamas,Rill, Attila,Balogh, Gabor,Vadasz, Zsolt,et al.

, p. 3213 - 3223 (2007/10/02)

Aminosuccinyl (Asu) peptides, containing a strained ring system, are very vulnerable to epimerization and, during their formation, even as transients, in the presence of nucleophilic and nonnucleophilic bases, partial epimerization occurs.In the presence

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