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L-Serine, N-[[2,3-dichloro-4-(2-methylene-1-oxobutyl)phenoxy]acetyl]is a chemical compound derived from the amino acid L-serine. It features an N-acetyl group attached to the amino group of L-serine, along with a phenoxy group that is substituted with dichloro and a 2-methylene-1-oxobutyl group. L-Serine, N-[[2,3-dichloro-4-(2-methylene-1-oxobutyl)phenoxy]acetyl]is known for its potential biological activities and is utilized in research and pharmaceutical applications. Its role as a substrate for enzymes and as a precursor for the synthesis of various biomolecules makes it a valuable asset in the development of new drugs and treatments. Furthermore, its chemical structure and properties are crucial for understanding the structure-activity relationships of similar compounds, which is essential for drug design and development.

113239-21-7

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113239-21-7 Usage

Uses

Used in Pharmaceutical Applications:
L-Serine, N-[[2,3-dichloro-4-(2-methylene-1-oxobutyl)phenoxy]acetyl]is used as a pharmaceutical precursor for the synthesis of various biomolecules. Its unique structure allows it to be a key component in the development of new drugs and treatments.
Used in Research Applications:
In research, L-Serine, N-[[2,3-dichloro-4-(2-methylene-1-oxobutyl)phenoxy]acetyl]is used as a substrate for enzymes, enabling scientists to study enzyme mechanisms and the synthesis of biomolecules. This helps in understanding the structure-activity relationships of similar compounds, which is vital for drug design and development.
Used in Drug Design and Development:
L-Serine, N-[[2,3-dichloro-4-(2-methylene-1-oxobutyl)phenoxy]acetyl]is used as a structural template in drug design and development. Its chemical properties and structure provide insights into the creation of new compounds with potential therapeutic effects, contributing to the advancement of pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 113239-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,3 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 113239-21:
(8*1)+(7*1)+(6*3)+(5*2)+(4*3)+(3*9)+(2*2)+(1*1)=87
87 % 10 = 7
So 113239-21-7 is a valid CAS Registry Number.

113239-21-7SDS

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-{[2,3-dichloro-4-(2-methylenebutyryl)phenoxy]-acetyl}-S(+)-serine

1.2 Other means of identification

Product number -
Other names (S)-2-{2-[2,3-Dichloro-4-(2-methylene-butyryl)-phenoxy]-acetylamino}-3-hydroxy-propionic 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:113239-21-7 SDS

113239-21-7Downstream Products

113239-21-7Relevant academic research and scientific papers

Discovery of glutathione S-transferase inhibitors using dynamic combinatorial chemistry

Shi, Baolu,Stevenson, Ross,Campopiano, Dominic J.,Greaney, Michael F.

, p. 8459 - 8467 (2007/10/03)

Protein-directed dynamic combinatorial chemistry (DCC) relies on reversible chemical reactions that can function under the near-physiological conditions required by the biological target. Few classes of reaction have so far proven effective at generating

Compounds useful in treating sickle cell anemia

-

, (2008/06/13)

The present invention is directed to compounds of the general formula I and pharmaceutically acceptable salts thereof: STR1 wherein R=H or lower alkyl; R'=H, lower alkyl, benzyl, CH2 OH; A=(CH2)1 to 5, >C(CH3)s

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