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Benzeneethanol, beta-amino-3-fluoro-, (betaS)(9CI) is a chiral chemical compound with the molecular formula C8H10FNO. It features a beta-amino alcohol structure with a fluorine atom substituted at the third carbon position. The (betaS) designation highlights the specific stereochemistry of the beta carbon, which is crucial for its potential applications in medicinal chemistry and pharmaceutical research. Its unique structure and properties make it a promising candidate for further studies to explore its potential uses and effects.

325152-98-5

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325152-98-5 Usage

Uses

Used in Medicinal Chemistry:
Benzeneethanol, beta-amino-3-fluoro-, (betaS)(9CI) is used as a building block in the synthesis of various pharmaceutical compounds. Its unique structure, including the fluorine substitution and chiral center, allows for the development of novel drugs with improved pharmacological properties.
Used in Pharmaceutical Research:
Benzeneethanol, beta-amino-3-fluoro-, (betaS)(9CI) serves as a valuable research tool in the field of pharmaceuticals. It can be used to investigate the effects of structural modifications on the biological activity of molecules, as well as to study the role of stereochemistry in drug design and development.
Used in Drug Discovery:
Benzeneethanol, beta-amino-3-fluoro-, (betaS)(9CI) is employed as a starting material or intermediate in the discovery of new drugs. Its unique structural features can be leveraged to design and synthesize compounds with specific therapeutic targets, potentially leading to the development of innovative treatments for various diseases.
Used in Drug Synthesis:
As a beta-amino alcohol with a fluorine substitution, Benzeneethanol, beta-amino-3-fluoro-, (betaS)- (9CI) can be utilized in the synthesis of various pharmaceutical agents. Its reactivity and functional groups can be exploited to create a wide range of drug candidates with diverse therapeutic applications.
Used in Chiral Chemistry:
The (betaS) designation of Benzeneethanol, beta-amino-3-fluoro-, (betaS)(9CI) highlights its importance in chiral chemistry. It can be used to study the effects of stereochemistry on the biological activity of compounds, as well as to develop enantioselective synthetic methods for the preparation of chiral pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 325152-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,1,5 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 325152-98:
(8*3)+(7*2)+(6*5)+(5*1)+(4*5)+(3*2)+(2*9)+(1*8)=125
125 % 10 = 5
So 325152-98-5 is a valid CAS Registry Number.
InChI:InChI=1S/C8H10FNO/c9-7-3-1-2-6(4-7)8(10)5-11/h1-4,8,11H,5,10H2/t8-/m1/s1

325152-98-5SDS

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 (S)-2-amino-2-(3-fluorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names (S)-2-Amino-2-(3-fluorophenyl)ethanol

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:325152-98-5 SDS

325152-98-5Relevant academic research and scientific papers

A general asymmetric synthesis of phenylglycinols

Pan, Xingang,Jia, Liangbin,Liu, Xuejian,Ma, Haikuo,Yang, Wenqian,Schwarz, Jacob B.

, p. 329 - 337 (2011/05/17)

Hydride reduction and deprotection of siloxymethyl sulfinimines 2 reliably furnished chiral phenylglycinols 1 or 10 in high overall yield and enantiomeric purity.

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