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4-(ethylsulfanyl)-4-phenylbutan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74896-58-5

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74896-58-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74896-58-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,9 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74896-58:
(7*7)+(6*4)+(5*8)+(4*9)+(3*6)+(2*5)+(1*8)=185
185 % 10 = 5
So 74896-58-5 is a valid CAS Registry Number.

74896-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethylsulfanyl-4-phenylbutan-2-one

1.2 Other means of identification

Product number -
Other names 4-ethylsulfanyl-4-phenyl-butan-2-one

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:74896-58-5 SDS

74896-58-5Relevant academic research and scientific papers

Ionic liquid catalysed reaction of thiols with α,β-unsaturated carbonyl compounds-remarkable influence of the C-2 hydrogen and the anion

Sarkar, Anirban,Roy, Sudipta Raha,Chakraborti, Asit K.

supporting information; scheme or table, p. 4538 - 4540 (2011/06/22)

Hydrogen bond induced reactivity and selectivity control in the 1-butyl-3-methylimidazolium based ionic liquid catalysed reaction of thiols with α,β-unsaturated carbonyl compounds is reported with remarkable influence of the anion and the C-2 hydrogen in

Scope and limitations of HClO4-SiO2 as an extremely efficient, inexpensive, and reusable catalyst for chemoselective carbon-sulfur bond formation

Khatik, Gopal L.,Sharma, Gaurav,Kumar, Raj,Chakraborti, Asit K.

, p. 1200 - 1210 (2007/10/03)

The scope and limitations of perchloric acid adsorbed on silica gel (HClO4-SiO2) as a highly efficient, inexpensive, and reusable catalyst for chemoselective carbon-sulfur bond formation by conjugate addition of thiols to α,β-unsatur

Thia-Michael addition reactions using 2-[bis(alkylthio)methylene]-3-oxo-N- o-tolylbutanamides as odorless and efficient thiol equivalents

Dong, Dewen,Yu, Haifeng,Ouyang, Yan,Liu, Qun,Bi, Xihe,Lu, Yumei

, p. 283 - 287 (2007/10/03)

A series of 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides 1 have been investigated as nonthiolic and odorless thiol equivalents in thia-Michael addition reactions. The cleavage of compounds 1 is initiated by NaOH in EtOH; the in situ generated th

Zinc perchlorate hexahydrate catalysed conjugate addition of thiols to α,β-unsaturated ketones

Garg, Sanjeev K.,Kumar, Raj,Chakraborti, Asit K.

, p. 1370 - 1374 (2007/10/03)

Zn(II) perchlorate hexahydrate has been found to be a new and efficient catalyst for conjugate addition of thiols to α,β-unsaturated ketones under solvent-free conditions at room temperature. The reaction of aryl, arylalkyl and alkyl thiols with cyclic an

Copper(II) tetrafluoroborate as a novel and highly efficient catalyst for Michael addition of mercaptans to α,β-unsaturated carbonyl compounds

Garg, Sanjeev K.,Kumar, Raj,Chakraborti, Asit K.

, p. 1721 - 1724 (2007/10/03)

Copper(II) tetrafluoroborate has been found to be a new and highly efficient catalyst for Michael addition of thiols to α,β-unsaturated carbonyl compounds under solvent-free conditions and in H2O at room temperature. The reactions are very fast

The reaction of some nuclear substituted acyclic conjugated styryl ketones and related Mannich bases with ethanethiol.

Dimmock, J.R.,Smith, L.M.,Smith, P.J.

, p. 984 - 991 (2007/10/02)

The second order rate constants for the reaction of ethanethiol with a number of conjugated nuclear-substituted styryl ketones and related Mannich bases in 50percent aqueous acetonitrile was undertaken.Variation of the alkyl group adjacent to the carbonyl

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