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19152-55-7

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19152-55-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19152-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,5 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19152-55:
(7*1)+(6*9)+(5*1)+(4*5)+(3*2)+(2*5)+(1*5)=107
107 % 10 = 7
So 19152-55-7 is a valid CAS Registry Number.

19152-55-7SDS

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 1-[4-(oxiran-2-ylmethoxy)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 1-[4-(2,3-Epoxy-propoxy)-phenyl]-aethanon

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:19152-55-7 SDS

19152-55-7Relevant articles and documents

Synthesis, antimicrobial and in vitro antitumor activities of a series of 1,2,3-thiadiazole and 1,2,3-selenadiazole derivatives

Mhaidat, Nizar M.,Al-Smadi, Mousa,Al-Momani, Fouad,Alzoubi, Karem H.,Mansi, Iman,Al-Balas, Qosay

, p. 3645 - 3652 (2015)

Three derivatives of substituted 1,2,3-thia- or 1,2,3-selenadiazole (4ac) were prepared and characterized by different chemical techniques. These compounds were evaluated for their antimicrobial and antitumor activities. Compounds 4a (propenoxide derivati

Regioselective Copper-Catalyzed Oxidative Coupling of α-Alkylated Styrenes with Tertiary Alkyl Radicals

Wang, Cong,Liu, Rui-Hua,Tian, Ming-Qing,Hu, Xu-Hong,Loh, Teck-Peng

supporting information, p. 4032 - 4035 (2018/07/15)

A radical-mediated oxidative cross-coupling of readily accessible α-alkylated styrenes with 1,3-dicarbonyl compounds utilizing a combination of Cu(OAc)2 and air as a catalytic system is described. Rather than requiring α-halocarbonyl compounds, this efficient approach enables direct installation of tertiary functionalized alkyl motifs to olefins with simple carbonyl derivatives. The novel protocol is characterized with high allylic selectivities via a competing β-H elimination. Both radical-clock and -trapping experiments provided clear-cut evidence for the intermediacy of an α-keto carbon-centered radical.

Thermally activated, single component epoxy systems

Unruh, David A.,Pastine, Stefan J.,Moreton, Jessica C.,Frechet, Jean M. J.

experimental part, p. 6318 - 6325 (2012/06/18)

A single component epoxy system in which the resin and hardener components found in many two-component epoxies are combined onto the same molecule is described. The single molecule precursor to the epoxy resin contains both multiple epoxide moieties and a

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