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

54513-99-4

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54513-99-4 Usage

Uses

A labelled intermediate in the synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 54513-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,1 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54513-99:
(7*5)+(6*4)+(5*5)+(4*1)+(3*3)+(2*9)+(1*9)=124
124 % 10 = 4
So 54513-99-4 is a valid CAS Registry Number.

54513-99-4SDS

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 3,3,4,4,5,5-hexadeuteriocyclohexan-1-one

1.2 Other means of identification

Product number -
Other names D6-cyclohexanone

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:54513-99-4 SDS

54513-99-4Relevant academic research and scientific papers

Synthesis of - and Lysines

Tsuzuki, Hirohisa,Mashimo, Takuya,Mukumoto, Mamoru,Mataka, Shuntaro,Udagawa, Jun,Tashiro, Masashi

, p. 2346 - 2360 (2007/10/03)

Starting from readily available cyclohexanone (1), synthesis of the title - and lysines (11) and (18) is described.Although direct incorporation of an amino or phthalimide group into the 2-bromohexanoic acid (5), which was derived from 1 in five steps. leading to 11 was unsuccessful due to hydrogen-deuterium scrambling, compound (11) was obtained in 86percent deuterium content via incorporation of an azido group and subsequent hydrogenation.Furthermore, compound (18) having 99percent deuterium content could be prepared by acid-catalysed deuterium exchange of 1 as a key-step.

Hydrogen Transfer Reactions, 19. - The Catalysis of Hydrogen Transfer and 1,5-H Shift by Rhodium(III) Chloride in Homogeneous Organic Systems

Wehage, Hubert,Heesing, Albert

, p. 209 - 215 (2007/10/02)

In homogeneous solution, partly in the presence of a phase-transfer catalyst, rhodium(III) chloride catalyzes the disproportionation of 1,3-cyclohexadiene and to a lesser extent 1,5-H shifts.In the start phase the catalyst is reduced to the active monovalent state.In these catalytic systems the dehydrogenation proceeds stereoselectively. - This was shown by tracer experiments and isotopes effects using deuterated 1,3-cyclohexadienes 1a-d, which were synthesized with high isotopomeric purity.Key Words: Rhodium chloride / Hydrogen transfer / Deuterated 1,3-cyclohexadienes / Isotope effects

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