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Phenol, 4-(1,1-dimethylethyl)-2-(ethylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64096-98-6

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64096-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64096-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,9 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64096-98:
(7*6)+(6*4)+(5*0)+(4*9)+(3*6)+(2*9)+(1*8)=146
146 % 10 = 6
So 64096-98-6 is a valid CAS Registry Number.

64096-98-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-butyl-2-ethylsulfanylphenol

1.2 Other means of identification

Product number -
Other names 2-ethylthio-4-t-butylphenol

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:64096-98-6 SDS

64096-98-6Relevant academic research and scientific papers

Process for preparing ortho-(alkylthio)phenols

-

, (2008/06/13)

The process of the invention involves reacting a phenol with a dialkyl disulfide in the presence of a zirconium phenoxide catalyst to prepare the corresponding ortho-(alkylthio)phenol.

2-(Aminomethyl)phenols, a new class of saluretic agents. I. Effect of nuclear substitution

Stokker,Deana,deSolms,Schultz,Smith,Cragoe Jr.,Baer,Ludden,Russo,Scriabine,Sweet,Watson

, p. 1414 - 1427 (2007/10/02)

A series of 2-(aminomethyl)phenols was synthesized and tested in rats and dogs for saluretic and diuretic activity. A number of these compounds exhibit a high order of activity on iv or po administration. The most active compounds belong to a subseries of 4-alkyl-6-halo derivatives of which 2,2(aminomethyl)-4-(1,1-dimethylethyl)-6-iodophenyl, is the most active. Compound 2 also possesses significant antihypertensive activity, an adjunctive pharmacological parameter which distinguishes 2 from the other compounds prepared in this series. In addition, 2 displays both topical saluretic and antiinflammatory activities.

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