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Benzene, [[(3-methyl-2-butenyl)oxy](methylthio)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112607-91-7

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112607-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112607-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,0 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112607-91:
(8*1)+(7*1)+(6*2)+(5*6)+(4*0)+(3*7)+(2*9)+(1*1)=97
97 % 10 = 7
So 112607-91-7 is a valid CAS Registry Number.

112607-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-methylbut-2-enoxy(methylsulfanyl)methyl]benzene

1.2 Other means of identification

Product number -
Other names Benzene,[[(3-methyl-2-butenyl)oxy](methylthio)methyl]

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:112607-91-7 SDS

112607-91-7Downstream Products

112607-91-7Relevant academic research and scientific papers

A Novel Synthesis of Phenylthiomethyl (PTM) Ethers and Esters by Anodic Oxidation of Phenyl Trimethylsilylmethyl Sulfide

Koizumi, Toshio,Fuchigami, Toshio,Nonaka, Tsutomu

, p. 1095 - 1096 (1987)

It was found that anodic oxidation of phenyl trimethylsilylmethyl sulfide in the presence of alcohols and carboxylic acids afforded various kinds of PTM ethers and esters, respectively, in good to reasonable yields.

Anodic Oxidation of (Trimethylsilyl)methanes with ?-Electron Substituents in the Presence of Nucleophiles

Koizumi, Toshio,Fuchigami, Toshio,Nonaka, Tsutomu

, p. 219 - 225 (2007/10/02)

It was found that oxidation potentials of methanes with ?-electron substituents were decreased by introduction of a trimethylsilyl group.The anodic oxidation of benzyl-, allyl-, aryl(or alkyl)thiomethyl-, and aryloxymethyl-substituted trimethylsilanes smoothly proceeded in the presence of nucleophiles, e.g. alcohols and carboxylic acids, to eliminate the trimethylsilyl groups giving the corresponding alkoxylated and carboxylated products in moderate or high yields without full optimization of electrolytic conditions, while aminomethylsilanes did not undergo such a kind of anodic oxidation.

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