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133863-87-3

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133863-87-3 Usage

General Description

2-Methoxy-6-(trifluoromethyl)aniline, also known as trifluoromethoxyaniline, is an aromatic amine containing a methoxy group and a trifluoromethyl group. It is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This chemical is also utilized in the production of dyes and pigments, as well as in the synthesis of various organic compounds. It is important to handle 2-methoxy-6-(trifluoromethyl)aniline with care as it is toxic if ingested, inhaled, or in contact with skin. It is also harmful to aquatic life and can have long-term effects on the environment. Proper safety and handling precautions should be followed when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 133863-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,6 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133863-87:
(8*1)+(7*3)+(6*3)+(5*8)+(4*6)+(3*3)+(2*8)+(1*7)=143
143 % 10 = 3
So 133863-87-3 is a valid CAS Registry Number.

133863-87-3SDS

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 2-Methoxy-6-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names 2-methoxy-6-trifluoromethylaniline

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:133863-87-3 SDS

133863-87-3Relevant articles and documents

A practical synthesis of 2-methoxy-6-trifluoromethylaniline

Pews, R. Garth

, p. 65 - 67 (1998)

A practical synthesis of 2-methoxy-6-trifluoromethylaniline is described via halogenation, nitration and reduction of 3-trifluoromethylanisole.

Preparation method of trifluoromethylamine

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Paragraph 0023-0026; 0027-0045; 0046-0056; 0076-0086, (2018/09/28)

The invention relates to a preparation method of trifluoromethylamine. The method includes the following steps that aromatic amine shown in the formula (1) and a trifluoromethyl reagent shown in the formula (2) react in a solvent under the condition that an alkali and/or nickel compound exists, and the trifluoromethylamine compound shown in the formula (3) is generated. According to the preparation method of trifluoromethylamine, aromatic amine and 1-trifluoromethyl-1,2-iodobenzoyl-3(H)-ketone serve as raw materials and react under the condition that the alkali and/or nickel compound exists through the amino positioning effect on aromatic nucleus. The synthesis steps of the method are simple, the cost of the raw materials is low, the production cost of trifluoromethylamine can be greatly reduced, and large-scale industrialized production is promoted.

THERAPEUTIC ARYL-AM I DO-ARYL COMPOUNDS AND THEIR USE

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Page/Page column 171-172, (2011/04/14)

The present invention pertains generally to the field of therapeutic compounds, and more specifically to certain aryl-amido-aryl compounds of the following formula (for convenience, collectively referred to herein as "AAA compounds"), which, inter alia, a

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