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N-Formyl-L-aspartic acid, also known as N-formylaspartic acid, is a chemical compound that belongs to the family of N-formylated amino acids. It is an intermediate in the biosynthesis of purine, a key component of DNA and RNA. N-Formyl-L-aspartic acid is formed through the formylation of L-aspartic acid and plays a crucial role in the synthesis of adenosine monophosphate (AMP), which is essential for energy transfer within cells. With its potential applications in pharmaceuticals and biochemistry, N-Formyl-L-aspartic acid is recognized as a precursor to important biological molecules and has been studied for its potential role in antimicrobial and antiviral therapies. It is also a target for drug development in the treatment of diseases such as cancer and metabolic disorders.

19427-28-2

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19427-28-2 Usage

Uses

Used in Pharmaceutical Industry:
N-Formyl-L-aspartic acid is used as a precursor in the synthesis of biologically important molecules for various pharmaceutical applications. Its role in the biosynthesis of purines makes it a valuable component in the development of drugs targeting diseases like cancer and metabolic disorders.
Used in Biochemical Research:
N-Formyl-L-aspartic acid is used as a research tool in biochemistry to study the mechanisms of purine biosynthesis and its implications in cellular energy transfer. It aids in understanding the fundamental processes of DNA and RNA synthesis, which are vital for life.
Used in Antimicrobial and Antiviral Therapies:
N-Formyl-L-aspartic acid is used as a potential agent in antimicrobial and antiviral therapies. Its unique structure and biochemical properties make it a candidate for developing new treatments against infectious diseases.
Used in Drug Development:
N-Formyl-L-aspartic acid is used as a target for drug development, focusing on its potential to treat various diseases. Its involvement in key biological pathways and its precursor role in essential molecules make it a promising candidate for creating novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 19427-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,2 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19427-28:
(7*1)+(6*9)+(5*4)+(4*2)+(3*7)+(2*2)+(1*8)=122
122 % 10 = 2
So 19427-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H7NO5/c7-2-6-3(5(10)11)1-4(8)9/h2-3H,1H2,(H,6,7)(H,8,9)(H,10,11)

19427-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-formyl-L-aspartic acid

1.2 Other means of identification

Product number -
Other names N-formyl-Asp-OH

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:19427-28-2 SDS

19427-28-2Relevant academic research and scientific papers

PROCESS FOR PRODUCING N-FORMYLAMINO ACID AND UTILIZATION THEREOF

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Page 12, (2008/06/13)

Provided is a process for producing an N- formylamino acid important as various synthetic intermediates at good efficiency and industrially easily by reacting an amino acid such as aspartic acid or a neutral amino acid with formamide and/or methyl formate in the presence of a base, or by reacting a salt of the amino acid with formamide and/or methyl formate.Further provided is a process for producing, at good efficiency and industrially easily, N-formyl-α-L-aspartyl-L-phenylalanine methyl ester as a precursor of a sweetener aspartame, and aspartame by further subjecting the ester to deformylation, in which in an enzyme condensation reaction of N-formyl-L-aspartic acid and/or its salt with L- and/or DL-phenylalanine methyl ester, an amount of water present in the reaction system is specified relative to the total weight amount of the reaction system.It is also possible to provide a process for producing high-purity N-formyl-α-L-aspartyl-L-phenylalanine methyl ester by subjecting a phenylalanine methyl ester adduct of N-formyl-α-L-aspartyl-L-phenylalanine methyl ester formed to pH adjustment.

N-formylation of amino carboxylic compounds with formamide

-

, (2008/06/13)

The amine nitrogen of an amino carboxylic acid is formylated by reacting the amino carboxylic acid with formamide.

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