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4-[(Aminocarbonyl)amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine is a complex chemical compound derived from the amino acid phenylalanine. It features an amino group, a carboxylic acid group, and a fluorenylmethoxy carbonyl protecting group. 4-[(AMinocarbonyl)aMino]-N-[(9H-fluoren-9-ylMethoxy)carbonyl]-D-phenylalanine may hold potential in medicinal chemistry, drug development, and research involving amino acid derivatives and peptide chemistry, although its specific properties and uses require further investigation and scientific study.

324017-22-3

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324017-22-3 Usage

Uses

Used in Medicinal Chemistry:
4-[(Aminocarbonyl)amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine is used as a building block for the synthesis of complex organic molecules and pharmaceutical compounds. Its unique structure, including the fluorenylmethoxy carbonyl protecting group, allows for versatile modifications and functionalization in the development of new drugs.
Used in Drug Development:
In the pharmaceutical industry, 4-[(Aminocarbonyl)amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine is utilized as a key intermediate in the synthesis of peptide-based therapeutics. Its presence in these compounds can influence their stability, solubility, and biological activity, making it a valuable component in the creation of novel medications.
Used in Amino Acid Derivative Research:
4-[(Aminocarbonyl)amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine serves as a subject of study in the field of amino acid chemistry, where researchers explore its reactivity, properties, and potential applications. Understanding its behavior can lead to the discovery of new synthetic routes and applications in various chemical processes.
Used in Peptide Chemistry Research:
In peptide chemistry, 4-[(Aminocarbonyl)amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine is employed as a component in the design and synthesis of peptides with specific functions. Its incorporation can affect the conformation, stability, and biological activity of the resulting peptides, which is crucial for their use in therapeutic and diagnostic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 324017-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,0,1 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 324017-22:
(8*3)+(7*2)+(6*4)+(5*0)+(4*1)+(3*7)+(2*2)+(1*2)=93
93 % 10 = 3
So 324017-22-3 is a valid CAS Registry Number.

324017-22-3SDS

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 (2R)-3-[4-(carbamoylamino)phenyl]-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:324017-22-3 SDS

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