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25889-36-5

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25889-36-5 Usage

General Description

3-Nitro-4-(trifluoromethyl)phenol is a chemical compound that belongs to the class of organic compounds known as nitrophenols. Nitrophenols refer to compounds that contain a phenol ring linked to a nitro group. 3-Nitro-4-(trifluoromethyl)phenol features a trifluoromethyl group, which contains one carbon atom and three fluorine atoms, attached to the phenol ring in addition to the nitro group. Due to the presence of these functional groups, 3-nitro-4-(trifluoromethyl)phenol exhibits certain characteristics and reactivity patterns commonly seen in other similar nitrophenols and trifluoromethyl compounds. Its properties are used in various applications in the chemical and pharmaceutical industries. The precise effects on human health and the environment are dependent on specific conditions of exposure and use.

Check Digit Verification of cas no

The CAS Registry Mumber 25889-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,8 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25889-36:
(7*2)+(6*5)+(5*8)+(4*8)+(3*9)+(2*3)+(1*6)=155
155 % 10 = 5
So 25889-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F3NO3/c8-7(9,10)5-2-1-4(12)3-6(5)11(13)14/h1-3,12H

25889-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-NITRO-4-(TRIFLUOROMETHYL)PHENOL

1.2 Other means of identification

Product number -
Other names 3-nitro-4-(trifluoromethyl)phenol

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:25889-36-5 SDS

25889-36-5Downstream Products

25889-36-5Relevant articles and documents

Oxidative nucleophilic substitution of hydrogen in nitroarenes with trifluoromethyl carbanions. Synthesis of trifluoromethyl phenols

Surowiec, Marek,Ma?kosza, Mieczys?aw

, p. 5019 - 5024 (2007/10/03)

Trifluoromethyl carbanions generated from the Ruppert reagent and TASF add to highly electron-deficient nitroarenes to produce σH adducts subsequently oxidized with dimethyldioxirane to substituted trifluoromethyl phenols.

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