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(S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol is a chemical compound that belongs to the class of amino alcohols. It contains an amine group and an alcohol group, with a phenyl ring substituted with a trifluoromethyl group. (S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol is characterized by its unique structure, which contributes to its diverse potential applications.

153181-07-8

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153181-07-8 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol is used as a key intermediate in the synthesis of pharmaceuticals for various therapeutic applications. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Development:
In the agrochemical industry, (S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol is used as a building block for the creation of novel compounds with potential applications in pest control, crop protection, and other agricultural areas. Its versatility in chemical reactions makes it a valuable asset in the design of new agrochemicals.
Used in Central Nervous System Disorder Treatment:
(S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol has been studied for its potential therapeutic applications, particularly in the treatment of central nervous system disorders. Its unique structure may allow for the development of new treatments with fewer side effects and improved patient outcomes.
Used in Inflammatory Disease Management:
In addition to its potential use in treating central nervous system disorders, (S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol has also been investigated for its potential in managing inflammation. Its unique properties may contribute to the development of new anti-inflammatory drugs with enhanced efficacy and reduced side effects.
Used in Materials Science:
(S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol may have applications in the field of materials science, such as in the development of new polymers and surfactants. Its unique structure and functional groups can be utilized to create novel materials with improved properties and performance.
Overall, (S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol is a versatile compound with diverse potential uses across various industries, making it a valuable asset for researchers and industry practitioners.

Check Digit Verification of cas no

The CAS Registry Mumber 153181-07-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,8 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 153181-07:
(8*1)+(7*5)+(6*3)+(5*1)+(4*8)+(3*1)+(2*0)+(1*7)=108
108 % 10 = 8
So 153181-07-8 is a valid CAS Registry Number.

153181-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-amino-3-(4-(trifluoromethyl)phenyl)propan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:153181-07-8 SDS

153181-07-8Relevant articles and documents

SUBSTITUTED AMINO TRIAZOLES USEFUL AS CHITINASE INHIBITORS

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Paragraph 0275; 0290; 0291; 0528, (2021/02/05)

Disclosed are amino triazole compounds of formula (I). These compounds are inhibitors of acidic mammalian chitinase and chitotriosidase. Also disclosed are methods of using the compounds to treat asthma reactions caused by allergens, as well as acute and chronic inflammatory diseases, autoimmune diseases, dental diseases, neurologic diseases, metabolic diseases, liver diseases, polycystic ovary syndrome, endometriosis, and cancer.

Variations of the Nature of the Chiral Auxiliary with a Highly Enantioselective Chiral NADH Model

Combret, Yves,Duflos, Jack,Dupas, Georges,Bourguignon, Jean,Queguiner, Guy

, p. 1635 - 1644 (2007/10/02)

Various chiral amine alcohols have been used as chiral auxiliares for a highly enantioselective NADH model.Some of these are new reagents which have been obtained by an enzymic resolution method.

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