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3,3-dimethyl-1-(methylthio)butan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39199-12-7

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39199-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39199-12-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,9 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39199-12:
(7*3)+(6*9)+(5*1)+(4*9)+(3*9)+(2*1)+(1*2)=147
147 % 10 = 7
So 39199-12-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H14OS/c1-7(2,3)6(8)5-9-4/h5H2,1-4H3

39199-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyl-1-(methylsulfanyl)butan-2-one

1.2 Other means of identification

Product number -
Other names 2-Butanone,3,3-dimethyl-1-(methylthio)

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:39199-12-7 SDS

39199-12-7Relevant academic research and scientific papers

Rh/DuanPhos-Catalyzed Asymmetric Hydrogenation of β-Acetylamino Vinylsulfides: An Approach to Chiral β-Acetylamino Sulfides

Gao, Wenchao,Lv, Hui,Zhang, Xumu

supporting information, p. 2877 - 2880 (2017/06/07)

Rh/DuanPhos-catalyzed asymmetric hydrogenation of challenging β-acetylamino vinylsulfides has been developed, affording chiral β-acetylamino sulfides with high yields and excellent ee's (up to 99% ee). This novel methodology provides an efficient and concise synthetic route to chiral β-acetylamino sulfides. The potential utility of this protocol in the synthesis of Apremilast has also been disclosed.

STEREOCHEMISTRY OF ORGANIC SULPHUR COMPOUNDS. PART 14 . SYNTHESIS AND CONFORMATION ANALYSIS OF 1-THIODERIVATIVES OF 3,3-DIMETHYL-2-BUTANOL AND ITS ACETATES.

Brunet, E.,Garcia-Ruano, J. L.,Rodriguez, J. H.,Alcudia, F.

, p. 4433 - 4445 (2007/10/02)

The synthesis and conformational analysis of some thioderivatives tBu-CHX-CH2Y (X = OH and OAc; Y = SH, SMe, SO2Me and SMe2) are reported.The conformational equilibria have been established from 1H NMR data and high dilution ir studies.All the compounds exhibited almost monoconformational behaviour around the C(1)-C(2) bond, due to strong steric factors.The observed vicinal coupling constants were used to check the different parameterizations of Altona's equation for our compounds with sulphur in distinct oxidation states.The possible dihedral angle deformations were also evaluated.

Method of preparing ketoxime carbamates

-

, (2008/06/13)

A novel process of preparing ketoxime carbamate.

Ketoxime carbamates

-

, (2008/06/13)

Carbamate derivatives of ketoximes are useful in combatting pests such as insects, mites, and nematodes.

Ketoxime carbamates

-

, (2008/06/13)

Carbamate derivatives of ketoximes are useful in combatting pests such as insects, mites, and nematodes.

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