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106877-48-9

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106877-48-9 Usage

Description

2-Amino-3-(trifluoromethyl)phenol is an organic compound characterized by the presence of an amino group, a trifluoromethyl group, and a phenol group. It is a versatile intermediate in the synthesis of various pharmaceutical compounds and can also be used in the preparation of pesticides.

Uses

Used in Pharmaceutical Industry:
2-Amino-3-(trifluoromethyl)phenol is used as an intermediate in the synthesis of pharmaceutical compounds, particularly inhibitors. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Pesticide Industry:
2-Amino-3-(trifluoromethyl)phenol is used in the preparation of pesticides with a trifluoromethyl moiety. Its presence in these compounds can enhance their effectiveness in controlling pests and improving crop yields.

Check Digit Verification of cas no

The CAS Registry Mumber 106877-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 106877-48:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*7)+(2*4)+(1*8)=149
149 % 10 = 9
So 106877-48-9 is a valid CAS Registry Number.

106877-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-3-(trifluoromethyl)phenol

1.2 Other means of identification

Product number -
Other names 2-HYDROXY-6-(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:106877-48-9 SDS

106877-48-9Downstream Products

106877-48-9Relevant articles and documents

Synthesis of 2-aminophenols and heterocycles by Ru-catalyzed C-H mono- and dihydroxylation

Yang, Xinglin,Shan, Gang,Rao, Yu

supporting information, p. 2334 - 2337 (2013/07/04)

A novel and efficient synthesis of 2-aminophenols, 2-aminobenzene-1,3- diols, and heterocycles through Ru-catalyzed C-H mono- and dihydroxylation of anilides has been developed with a new directing group strategy. The reaction demonstrates excellent reactivity, regioselectivity, good functional group tolerance, and high yields.

Reactions of Trifluoromethyl Bromide and Related Halides: Part 10. Perfluoroalkylation of Aromatic Compounds induced by Sulphur Dioxide Radical Anion Precursors

Tordeux, Marc,Langlois, Bernard,Wakselman, Claude

, p. 2293 - 2299 (2007/10/02)

Perfluoroalkylation of electron-rich aromatic compounds with trifluoromethyl bromide, or long-chain perfluoroalkyl iodides, was performed in the presence of sodium dithionite or zinc-sulphur dioxide.This alkylation occurred at the ortho and para positions relative to the amino or hydroxy substitutent.Pyrroles were perfluoroalkylated regioselectively at the 2-position.This alkylation was interpreted as a radical aromatic substitution; the formation of the perfluoroalkyl radical can be induced by a single-electron transfer from sulphur dioxide radical anion to the perfluoroalkyl halide.

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