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35852-57-4

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35852-57-4 Usage

Type of compound

Phenolic compound

Constituents

Two bromine atoms, a trifluoromethyl group, and a phenol ring

Usage

Building block for pharmaceuticals, agrochemicals, and specialty chemicals

Application

Intermediate in the production of dyes, pigments, and other organic compounds

Properties

Antimicrobial, antifungal, and antioxidant

Potential use

Development of new drugs and bioactive compounds

Safety concerns

Toxic and potentially hazardous nature, requiring proper handling and safety precautions

Check Digit Verification of cas no

The CAS Registry Mumber 35852-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,5 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35852-57:
(7*3)+(6*5)+(5*8)+(4*5)+(3*2)+(2*5)+(1*7)=134
134 % 10 = 4
So 35852-57-4 is a valid CAS Registry Number.

35852-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dibromo-4-(trifluoromethyl)phenol

1.2 Other means of identification

Product number -
Other names 2,6-dibromo-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:35852-57-4 SDS

35852-57-4Relevant articles and documents

A Bulky Thiyl-Radical Catalyst for the [3+2] Cyclization of N-Tosyl Vinylaziridines and Alkenes

Hashimoto, Takuya,Takino, Kohei,Hato, Kazuki,Maruoka, Keiji

supporting information, p. 8081 - 8085 (2016/09/13)

Thiyl-radical-catalyzed cyclization reactions of N-tosyl vinylaziridines and alkenes were developed as a new synthetic method for the generation of substituted pyrrolidines. The key to making this process accessible to a broad range of substrates is the use of a sterically demanding thiyl radical, which prevents the undesired degradation of the catalyst.

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