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2,2-DIMETHYL-2'-THIOMETHYLPROPIOPHENONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

507272-92-6

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507272-92-6 Usage

Common uses

Photoinitiator in UV-curable coatings, inks, and adhesives; production of polymer materials; chemical intermediate in organic synthesis

Photopolymerization

Rapid reaction when exposed to ultraviolet light leading to crosslinking of polymers in coatings or adhesives

Benefits

Faster curing times and improved performance of coatings and adhesives

Safety concerns

Potential health and safety risks if not used properly

Check Digit Verification of cas no

The CAS Registry Mumber 507272-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,7,2,7 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 507272-92:
(8*5)+(7*0)+(6*7)+(5*2)+(4*7)+(3*2)+(2*9)+(1*2)=146
146 % 10 = 6
So 507272-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H16OS/c1-12(2,3)11(13)9-7-5-6-8-10(9)14-4/h5-8H,1-4H3

507272-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-1-(2-methylsulfanylphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 2,2-DIMETHOXY-1-PIPERIDIN-1-YLETHAN-1-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:507272-92-6 SDS

507272-92-6Downstream Products

507272-92-6Relevant articles and documents

Chiral phosphoric acid catalyzed asymmetric transfer hydrogenation of bulky aryl ketones with ammonia borane

Zhou, Qiwen,Meng, Wei,Feng, Xiangqing,Du, Haifeng,Yang, Jing

supporting information, (2019/11/28)

An asymmetric transfer hydrogenation of bulky aryl ketones with ammonia borane was successfully realized with chiral phosphoric acid (CPA) as catalyst and water as additive. A variety of optically active secondary alcohols were obtained in good to high yi

Synthesis and reactivity of aryl- and heteroaryl-magnesium reagents bearing keto groups

Kneisel, Florian Felix,Knochel, Paul

, p. 1799 - 1802 (2007/10/03)

The reaction of iodophenyl ketones with neo-pentylmagnesium bromide in THF or THF:NMP or THF:DMAC mixtures allows the first preparation of aryl- and heteroarylmagnesium species bearing a ketone. Under appropriate conditions, these new reagents react with

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