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(2S)-amino[(4S,5R)-3-chloro-4-hydroxy-4,5-dihydro-1,2-oxazol-5-yl]ethanoic acid is a complex organic molecule derived from the amino acid glycine. It features an amino group and a carboxylic acid group, along with a 1,2-oxazol-5-yl ring that has a chlorine and hydroxyl group attached. The stereochemistry of the compound is defined by the (2S) and (4S,5R) designations, which describe the arrangement of atoms around the chiral centers. This unique structure may offer potential applications in medicine, pharmacology, and biochemistry, although further research is required to fully explore its properties and uses.

54549-02-9

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54549-02-9 Usage

Uses

Used in Pharmaceutical Industry:
(2S)-amino[(4S,5R)-3-chloro-4-hydroxy-4,5-dihydro-1,2-oxazol-5-yl]ethanoic acid is used as a potential pharmaceutical compound for its unique structural features. The presence of the amino and carboxylic acid groups, along with the 1,2-oxazol-5-yl ring and its substituents, may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Biochemical Research:
In the field of biochemistry, (2S)-amino[(4S,5R)-3-chloro-4-hydroxy-4,5-dihydro-1,2-oxazol-5-yl]ethanoic acid can be utilized as a research tool to study enzyme interactions, protein binding, and other biochemical processes. Its specific stereochemistry and functional groups may provide insights into the mechanisms of various biological reactions.
Used in Medicinal Chemistry:
(2S)-amino[(4S,5R)-3-chloro-4-hydroxy-4,5-dihydro-1,2-oxazol-5-yl]ethanoic acid may serve as a building block or a template in the design of new pharmaceuticals. Its unique structure could be exploited to create novel molecules with specific therapeutic effects, potentially leading to the development of innovative treatments for various diseases.
Note: The specific applications mentioned above are hypothetical and provided as examples based on the compound's structural features. Actual uses would depend on the results of further research and development in the relevant fields.

Check Digit Verification of cas no

The CAS Registry Mumber 54549-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,4 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54549-02:
(7*5)+(6*4)+(5*5)+(4*4)+(3*9)+(2*0)+(1*2)=129
129 % 10 = 9
So 54549-02-9 is a valid CAS Registry Number.

54549-02-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-2-[(4S,5R)-3-chloro-4-hydroxy-4,5-dihydro-1,2-oxazol-5-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 4-Hydroxyacivicin

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:54549-02-9 SDS

54549-02-9Downstream Products

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