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

64732-18-9

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64732-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64732-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,3 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64732-18:
(7*6)+(6*4)+(5*7)+(4*3)+(3*2)+(2*1)+(1*8)=129
129 % 10 = 9
So 64732-18-9 is a valid CAS Registry Number.

64732-18-9SDS

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 1-methyl-4-prop-2-ynylsulfinylbenzene

1.2 Other means of identification

Product number -
Other names 4-methylphenyl prop-2-ynyl sulfoxide

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:64732-18-9 SDS

64732-18-9Relevant academic research and scientific papers

Selective oxidation method of thioether

-

Paragraph 0054; 0055; 0056, (2018/09/20)

The invention relates to a selective oxidation method of thioether, and discloses a novel synthesis method of a single sulfone compound shown as a formula (I). According to the invention, thioether shown in a formula (II) is taken as a raw material, under existence of tert-butyl hydroperoxide, an oxidation reaction is carried out in a solvent, after the reaction is completed, and through post-treatment, the single sulfone compound shown as the formula (I) is obtained. Compared with the prior art, an oxidizing agent tert-butyl hydroperoxide which is friendly to environment is employed, usage ofa metal catalyst is avoided, the reaction condition is mild, selectivity is high, the operation is simple, the applicability is wide, and the reaction yield is high.

Copper-catalyzed asymmetric oxidation of sulfides

O'Mahony, Graham E.,Ford, Alan,Maguire, Anita R.

, p. 3288 - 3296 (2012/05/20)

Copper-catalyzed asymmetric sulfoxidation of aryl benzyl and aryl alkyl sulfides, using aqueous hydrogen peroxide as the oxidant, has been investigated. A relationship between the steric effects of the sulfide substituents and the enantioselectivity of th

Benzo(b)thiophene derivatives and process for producing the same

-

, (2008/06/13)

The present invention is 3,4-disubstituted-benzo[b]thiophene derivatives represented by general formula (I) and processes for preparing compounds represented by general formula (V) from compounds represented by general formula (IV), preparing a mixture of compounds represented by the following formula (II) and the following formula (III) and preparing the benzo[b]thiophene derivatives represented by the above formula (I). wherein, R1 and R2 represent each a halogen atom, a trihalomethyl group, a C1-4 alkyl group or a C14 alkoxy group; X represents a hydroxy group or a halogen atom; R3 and R4 represent each a hydrogen or a halogen atom, a trihalomethyl group, a C1-4 alkyl group or a C1-4 alkoxy group; and R5 represents a C1-3 alkyl group or a trifluoromethyl group.

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