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5106-00-3

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5106-00-3 Usage

Description

(S)-METHYL 3-(4-HYDROXY-3-NITROPHENYL)-2-(2,2,2-TRIFLUOROACETYLAMINO)PROPIONATE is a complex chemical compound with a unique structure, consisting of a methyl group, a hydroxy-nitrophenyl group, and a trifluoroacetylamino group bonded to a propionate backbone. This synthetic compound holds potential in the pharmaceutical industry, particularly for the development of novel drugs to address various medical conditions. Further research and testing are necessary to explore its full potential, benefits, and risks.

Uses

Used in Pharmaceutical Industry:
(S)-METHYL 3-(4-HYDROXY-3-NITROPHENYL)-2-(2,2,2-TRIFLUOROACETYLAMINO)PROPIONATE is used as a key intermediate in the synthesis of new drugs for various medical conditions. Its unique structure and functional groups make it a promising candidate for the development of innovative therapeutic agents.
Used in Drug Design and Development:
In the field of drug design and development, (S)-METHYL 3-(4-HYDROXY-3-NITROPHENYL)-2-(2,2,2-TRIFLUOROACETYLAMINO)PROPIONATE serves as a valuable building block for creating novel molecular entities. Its incorporation into drug candidates can potentially enhance their pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Medicinal Chemistry Research:
(S)-METHYL 3-(4-HYDROXY-3-NITROPHENYL)-2-(2,2,2-TRIFLUOROACETYLAMINO)PROPIONATE is utilized as a research tool in medicinal chemistry to study the structure-activity relationships of various drug candidates. Understanding how this compound interacts with biological targets can provide insights into the design of more effective and safer medications.
Used in Drug Synthesis and Optimization:
As a synthetic compound, (S)-METHYL 3-(4-HYDROXY-3-NITROPHENYL)-2-(2,2,2-TRIFLUOROACETYLAMINO)PROPIONATE is employed in the synthesis of diverse drug molecules. Its unique structural features can be exploited to optimize the pharmacokinetic and pharmacodynamic properties of drug candidates, potentially leading to improved therapeutic outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 5106-00-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5106-00:
(6*5)+(5*1)+(4*0)+(3*6)+(2*0)+(1*0)=53
53 % 10 = 3
So 5106-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H11F3N2O6/c1-23-10(19)7(16-11(20)12(13,14)15)4-6-2-3-9(18)8(5-6)17(21)22/h2-3,5,7,18H,4H2,1H3,(H,16,20)/t7-/m0/s1

5106-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-3-(4-hydroxy-3-nitrophenyl)-2-[(2,2,2-trifluoroacetyl)amino]propanoate

1.2 Other means of identification

Product number -
Other names (S)-METHYL 3-(4-HYDROXY-3-NITROPHENYL)-2-(2,2,2-TRIFLUOROACETYLAMINO)PROPIONATE

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:5106-00-3 SDS

5106-00-3Relevant articles and documents

Convenient synthesis of 3-fluoro-L-tyrosine and 3,5-difluoro-L-tyrosine

Kirk

, p. 2015 - 2016 (2007/10/02)

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