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Benzenamine, N-ethyl-3-(trifluoromethyl)-, also known as 3-(trifluoromethyl)-N-ethylaniline or 3-ethyl-N-(trifluoromethyl)aniline, is an organic compound with the chemical formula C9H10F3N. It is a derivative of aniline, featuring a trifluoromethyl group at the 3-position and an ethyl group at the nitrogen atom. This colorless liquid is soluble in organic solvents and has a molecular weight of 193.18 g/mol. It is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential reactivity and the presence of the trifluoromethyl group, it is important to handle Benzenamine, N-ethyl-3-(trifluoromethyl)- with care, following appropriate safety measures.

774-98-1

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774-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 774-98-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 774-98:
(5*7)+(4*7)+(3*4)+(2*9)+(1*8)=101
101 % 10 = 1
So 774-98-1 is a valid CAS Registry Number.

774-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-3-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names N-ethyl-3-trifluoromethyl-aniline

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:774-98-1 SDS

774-98-1Relevant academic research and scientific papers

Mild catalytic deoxygenation of amides promoted by thorium metallocene

Eisen, Moris S.,Saha, Sayantani

supporting information, p. 12835 - 12841 (2020/10/05)

The organoactinide-catalyzed (Cp*2ThMe2) hydroborated reduction of a wide range of tertiary, secondary, and primary amides to the corresponding amines/amine-borane adductsviadeoxygenation of the amides is reported herein. The catalytic reactions proceed under mild conditions with low catalyst loading and pinacolborane (HBpin) concentration in a selective fashion. Cp*2ThMe2is capable of efficiently catalysing the gram-scale reaction without a drop in efficiency. The amine-borane adducts are successfully converted into free amine products in high conversions, which increases the usefulness of this catalytic system. A plausible mechanism is proposed based on detailed kinetics, stoichiometric, and deuterium labeling studies.

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