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342621-21-0

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342621-21-0 Usage

Description

2-Trifluoroacetyl-4-chloro-5-triisopropylsilyloxyaniline is a complex organic compound characterized by its unique molecular structure, which features a trifluoroacetyl group, a chloro substituent, and a triisopropylsilyl ether moiety attached to an aniline core. 2-Trifluoroacetyl-4-chloro-5-triisopropylsilyloxyaniline is known for its potential applications in various chemical processes and industries.

Uses

Used in Organic Synthesis:
2-Trifluoroacetyl-4-chloro-5-triisopropylsilyloxyaniline is used as a synthetic intermediate for the preparation of various organic compounds. Its unique functional groups and structural features make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Trifluoroacetyl-4-chloro-5-triisopropylsilyloxyaniline is used as a key intermediate in the synthesis of novel drug candidates. Its presence in the molecular structure can impart specific biological activities and improve the pharmacokinetic properties of the final drug molecules.
Used in Agrochemical Industry:
2-Trifluoroacetyl-4-chloro-5-triisopropylsilyloxyaniline is also utilized in the agrochemical industry for the development of new pesticides and herbicides. Its incorporation into the molecular structure of these compounds can enhance their efficacy and selectivity, leading to improved crop protection.
Used in Specialty Chemicals:
In the specialty chemicals sector, 2-Trifluoroacetyl-4-chloro-5-triisopropylsilyloxyaniline is employed as a versatile intermediate for the synthesis of various high-value chemicals. Its unique properties can be exploited to create innovative materials with specific applications in areas such as coatings, adhesives, and polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 342621-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,6,2 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 342621-21:
(8*3)+(7*4)+(6*2)+(5*6)+(4*2)+(3*1)+(2*2)+(1*1)=110
110 % 10 = 0
So 342621-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H25ClF3NO2Si/c1-9(2)25(10(3)4,11(5)6)24-15-8-14(22)12(7-13(15)18)16(23)17(19,20)21/h7-11H,22H2,1-6H3

342621-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-amino-5-chloro-4-tri(propan-2-yl)silyloxyphenyl]-2,2,2-trifluoroethanone

1.2 Other means of identification

Product number -
Other names 2-Trifluoroacetyl-4-chloro-5-triisopropylsilyloxyaniline

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:342621-21-0 SDS

342621-21-0Downstream Products

342621-21-0Relevant articles and documents

Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor efavirenz

Markwalder, Jay A.,Christ, David D.,Mutlib, Abdul,Cordova, Beverly C.,Klabe, Ronald M.,Seitz, Steven P.

, p. 619 - 622 (2007/10/03)

Studies on the biotransformation of the clinically important non-nucleoside reverse transcriptase inhibitor efavirenz have shown that oxidation and secondary conjugation are important components of the processing of this molecule in vivo. We have synthesized metabolites of efavirenz to confirm their structure and to evaluate their activity as antivirals.

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