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Phenol, 4-[[4-(trifluoromethyl)phenyl]thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53451-92-6

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53451-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53451-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,5 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53451-92:
(7*5)+(6*3)+(5*4)+(4*5)+(3*1)+(2*9)+(1*2)=116
116 % 10 = 6
So 53451-92-6 is a valid CAS Registry Number.

53451-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[4-(trifluoromethyl)phenyl]sulfanylphenol

1.2 Other means of identification

Product number -
Other names 4-{[4-(trifluoromethyl)phenyl]thio}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:53451-92-6 SDS

53451-92-6Downstream Products

53451-92-6Relevant academic research and scientific papers

Preparation method of pyriproxyfen compounds

-

Paragraph 0079; 0080; 0081, (2016/10/27)

The invention provides a compound shown in structural formula I as well as stereoisomer, solvate and salt of the compound. In the structural formula I, R1 is selected from fluorine, chlorine, a cyano group or perfluoro-substituted C1-C3 alkyl; R2 is selected from hydrogen or C1-C3 alkyl; each of R3 and R4 is independently selected from hydrogen, C1-C3 alkyl, fluorine, chlorine or perfluoro-substituted C1-C3 alkyl; X is selected from O, S or -CH2-. The invention further provides a preparation method of the compound and an application of the compound in killing of harmful insects, public health epidemic prevention, control of plant diseases and insect pests and animal health care.

Solid-phase synthesis of diaryl sulfides: Direct coupling of solid-supported aryl halides with thiols using an insoluble polymer-supported reagent

Gendre, Fabrice,Yang, Mathieu,Diaz, Philippe

, p. 2719 - 2722 (2007/10/03)

(Chemical Equation Presented) Diaryl sulfides have been prepared by direct nickel(II)-catalyzed coupling of thiols with iodoaryl bound to SynPhase polystyrene lanterns in the presence of polymer-supported borohydride.

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