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121307-27-5

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121307-27-5 Usage

General Description

Benzenamine, 4-ethoxy-2-(trifluoromethyl)- (9CI) is a chemical compound with the molecular formula C10H10F3NO. It is also known by its CAS number 54007-97-3. This chemical is a derivative of aniline and is characterized by a trifluoromethyl group and an ethoxy group attached to the benzene ring. It is commonly used in organic synthesis and pharmaceutical research as a building block in the production of various compounds. Its properties and potential uses are of interest in the field of chemistry and drug development. However, as with any chemical, proper handling and safety precautions should be taken when working with Benzenamine, 4-ethoxy-2-(trifluoromethyl)- (9CI) to prevent any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 121307-27-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,3,0 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121307-27:
(8*1)+(7*2)+(6*1)+(5*3)+(4*0)+(3*7)+(2*2)+(1*7)=75
75 % 10 = 5
So 121307-27-5 is a valid CAS Registry Number.

121307-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Ethoxy-2-(trifluoromethyl)aniline

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:121307-27-5 SDS

121307-27-5Downstream Products

121307-27-5Relevant articles and documents

Ruthenium-Catalyzed Site-Selective Trifluoromethylations and (Per)Fluoroalkylations of Anilines and Indoles

Li, Yang,Neumann, Helfried,Beller, Matthias

supporting information, p. 6784 - 6788 (2020/05/18)

Introducing (per)fluoroalkyl groups into arenes continues to be an interesting, but challenging area in organofluorine chemistry. We herein report an ortho-selective C?H perfluoroalkylation including trifluoromethylations of anilines and indoles without the need of protecting groups using RfI and RfBr as commercially available reagents. The availability and price of the starting materials and the inherent selectivity make this novel methodology attractive for the synthesis of diverse (per)fluoroalkylated building blocks, for example, for bioactive compounds and materials.

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