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(2,3-D2)-1-Phenoxypropan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73811-48-0

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73811-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73811-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,1 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73811-48:
(7*7)+(6*3)+(5*8)+(4*1)+(3*1)+(2*4)+(1*8)=130
130 % 10 = 0
So 73811-48-0 is a valid CAS Registry Number.

73811-48-0Upstream product

73811-48-0Downstream Products

73811-48-0Relevant articles and documents

Ambient Hydrogenation and Deuteration of Alkenes Using a Nanostructured Ni-Core–Shell Catalyst

Beller, Matthias,Feng, Lu,Gao, Jie,Jackstell, Ralf,Jagadeesh, Rajenahally V.,Liu, Yuefeng,Ma, Rui

, p. 18591 - 18598 (2021)

A general protocol for the selective hydrogenation and deuteration of a variety of alkenes is presented. Key to success for these reactions is the use of a specific nickel-graphitic shell-based core–shell-structured catalyst, which is conveniently prepared by impregnation and subsequent calcination of nickel nitrate on carbon at 450 °C under argon. Applying this nanostructured catalyst, both terminal and internal alkenes, which are of industrial and commercial importance, were selectively hydrogenated and deuterated at ambient conditions (room temperature, using 1 bar hydrogen or 1 bar deuterium), giving access to the corresponding alkanes and deuterium-labeled alkanes in good to excellent yields. The synthetic utility and practicability of this Ni-based hydrogenation protocol is demonstrated by gram-scale reactions as well as efficient catalyst recycling experiments.

Homogeneous Deuteriation of Alkenes using (X = halide, R = aryl) Catalysts

Guengoer, Muammer,Jardine, Fred H.,Wheatley, J. Denis

, p. 1653 - 1656 (2007/10/02)

Catalytic deuteriation of cycloalkenes using (X = halide, R = aryl) catalysts frequently gives rise to some polydeuteriation and scrambled addition of deuterium to the cycloalkene substrate.It is shown that these undesirable side reactions can

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