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Oxirane, 2-[(4-chlorophenoxy)methyl]-2-(1,1-dimethylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80443-61-4

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80443-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80443-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,4,4 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80443-61:
(7*8)+(6*0)+(5*4)+(4*4)+(3*3)+(2*6)+(1*1)=114
114 % 10 = 4
So 80443-61-4 is a valid CAS Registry Number.

80443-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butyl-2-[(4-chlorophenoxy)methyl]oxirane

1.2 Other means of identification

Product number -
Other names 2-(4-chlorophenoxy-methyl)-2-tert-butyl-oxirane

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:80443-61-4 SDS

80443-61-4Relevant academic research and scientific papers

Synthesis of Vicinal Quaternary All-Carbon Centers via Acid-catalyzed Cycloisomerization of Neopentylic Epoxides

Schmid, Matthias,Sokol, Kevin R.,Wein, Lukas A.,Torres Venegas, Sofia,Meisenbichler, Christina,Wurst, Klaus,Podewitz, Maren,Magauer, Thomas

supporting information, p. 6526 - 6531 (2020/09/02)

We report our studies on the development of a catalytic cycloisomerization of 2,2-disubstituted neopentylic epoxides to produce highly substituted tetralins and chromanes. Termination of the sequence occurs via Friedel-Crafts-type alkylation of the remote (hetero)arene linker. The transformation is efficiently promoted by sulfuric acid and proceeds best in 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) as the solvent. Variation of the substitution pattern provided detailed insights into the migration tendencies and revealed a competing disproportionation pathway of dihydronaphthalenes.

Process for the preparation of oxiranes

-

, (2008/06/13)

A process for the preparation of oxiranes is disclosed in which a ketone of the formula STR1 wherein Y represents chlorine or phenyl, X represents oxygen or CH2 and Z represents hydrogen or halogen is reacted with trimethylsulphonium methyl sulphate formed by treating dimethyl sulphide with dimethyl sulphate. The process is carried out in the presence of potassium hydroxide or sodium hydroxide powder in an inert organic diluent at 0° to 60° C. The products are useful as intermediates for the formation of plant growth regulants and fungicides.

Antimicrobial azoles

-

, (2008/06/13)

The invention relates to 1-hydroxylethyl-azole derivatives of formula (I) in composition form and includes the use of such compositions as antimicrobial agents.

Antiviral agents

-

, (2008/06/13)

The invention relates to hydroxyethylazolyl derivatives, defined herein by formula (I) and particularly to the use of said derivatives for the treatment of viral infections.

Synergistic compositions for inhibiting plant growth

-

, (2008/06/13)

A plant growth-inhibiting composition comprising STR1 wherein the various radicals are as defined.

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