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STYRENE-ALPHA,2,3,4,5,6-D6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

217501-55-8

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217501-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 217501-55-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,7,5,0 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 217501-55:
(8*2)+(7*1)+(6*7)+(5*5)+(4*0)+(3*1)+(2*5)+(1*5)=108
108 % 10 = 8
So 217501-55-8 is a valid CAS Registry Number.

217501-55-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5-pentadeuterio-6-(1-deuterioethenyl)benzene

1.2 Other means of identification

Product number -
Other names Styrene-|A,2,3,4,5,6-d6

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:217501-55-8 SDS

217501-55-8Relevant academic research and scientific papers

Oxidative Dehydrogenation on Nanocarbon: Revealing the Reaction Mechanism via In Situ Experimental Strategies

Wang, Chao,Liu, Wei,Wei, Shimeng,Su, Dangsheng,Qi, Wei

, p. 397 - 400 (2018/11/23)

Classical mechanistic analysis strategy, including active site chemical titration, kinetic measurement and corresponding isotopic effect and surface reaction of single reactant etc., were performed in oxidative dehydrogenation reactions on nanocarbon. The

Mild and selective H/D exchange at the β position of aromatic α-olefins by N-heterocyclic carbene-hydride-rhodium catalysts

Di Giuseppe, Andrea,Castarlenas, Ricardo,Perez-Torrente, Jesus J.,Lahoz, Fernando J.,Polo, Victor,Oro, Luis A.

supporting information; experimental part, p. 3938 - 3942 (2011/06/24)

Pacman bites selectively! Stable rhodium(III)-N-heterocyclic carbene-hydride complexes (Pacman-like catalysts) are highly active and selective catalysts for H/D exchange at the β position of aromatic α-olefins (see picture). The interplay between bulky N-

Nanocarbon as robust catalyst: Mechanistic insight into carbon-mediated catalysis

Zhang, Jian,Su, Dangsheng,Zhang, Aihua,Wang, Di,Schloegl, Robert,Hebert, Cecile

, p. 7319 - 7323 (2008/09/18)

(Figure Presented) Kicking the coke habit: In nanocarbon-catalyzed oxidative dehydrogenation of ethylbenzene, oxygen is dissociatively adsorbed, and breaking of C-H bonds in ethylbenzene is kinetically relevant. In contrast to metal-based catalysts, the subsurface structure plays no role in the activity of the nanocarbon catalyst. Unlike activated carbon, the nanocarbon catalysts show no loss of activity from coking or combustion.

Screening catalysts for the catalytic exchange of hydrogen by tritium using magnetic labeling

Niessen, Heiko G.,Ulrich, Claudia,Bargon, Joachim

, p. 711 - 720 (2007/10/03)

Isotope labeling is an important method to evaluate drugs and compounds for agricultural use. Therefore, a fast and convenient method to selectively exchange hydrogen against non-radioactive deuterium or radioactive tritium in the final product is desirable. PHIP-NMR investigations of the influence of CO on the selective exchange of the geminal protons in styrene show that CO increases the efficiency of the selective exchange non-linearly and suppresses the hydrogenation of styrene to ethylbenzene.

PREPARATION OF DEUTERIATED 1-PHENYLETHANOLS BY REDUCTIVE DEHALOGENATION OF THE CORRESPONDING HALOGENOACETOPHENONES WITH RANEY ALLOYS IN AN ALKALINE DEUTERIUM OXIDE SOLUTION

Tashiro, Masashi,Mataka, Shuntaro,Nakamura, Hiroshi,Nakayama, Kouji

, p. 179 - 182 (2007/10/02)

Deuteriated 1-phenylethanols were prepared by reductive dehalogenation of the corresponding halogenoacetophenones with Raney Ni-Al and Cu-Al alloys in 5percent NaOD-D2O solution.It was found that the Ni-Al alloy introduced greater than expected numbers of deuterium atoms in the phenyl ring, but the expected deuteriated 1-phenylethanols were obtained in high yield and in high isotopic purity when Raney Cu-Al alloy was used.

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