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2-benzoyl-2-dimethylamino-3-phenylpropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69262-52-8

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69262-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69262-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,6 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69262-52:
(7*6)+(6*9)+(5*2)+(4*6)+(3*2)+(2*5)+(1*2)=148
148 % 10 = 8
So 69262-52-8 is a valid CAS Registry Number.

69262-52-8Relevant academic research and scientific papers

Enantioselective [1,2]-Stevens rearrangement using sugar-derived alkoxides as chiral promoters

Tomooka, Katsuhiko,Sakamaki, Junichiro,Harada, Manabu,Wada, Ryoji

, p. 683 - 686 (2008/12/20)

The first example of enantioselective base-induced [1,2]-Stevens rearrangement was achieved by using the newly developed D-glucose-derived lithium alkoxide as a chiral promoter. This rearrangement provides an α-amino ketone having a pseudoquaternary chira

Novel alpha-aminoacetophenones as photoinitiators

-

, (2008/06/13)

Compounds of the formula I, II, III and IIIa STR1 in which Ar1 is an unsubstituted or substituted aromatic radical and at least one of the radicals R1 and R2 is an alkenyl, cycloalkenyl or arylmethyl group, are effective photoinitiators for photopolymerization of unsaturated compounds. They are particularly suitable for photocuring of pigmented systems.

Base Catalysed Rearrangements involving Ylide Intermediates. Part 18. Competing , , and Rearrangements of Ammonium Ylides

Chantrapromma, Kan,Ollis, W. David,Sutherland, Ian O.

, p. 1049 - 1062 (2007/10/02)

The rearrangements of acyl stabilised ammonium ylides are, in several cases, accompanied by competing rearrangements and in one case by a rearrangement.For examples involving migrating benzyl or phenylethyl groups the mechanism of these rearrangements has been studied.Thus the competing , , and rearrangements of the ylide (12) are largely intramolecular, but the intermolecularity is as high as 28percent for the and rearrangements and 14percent for the rearrangement in methanol at 55 deg C.The competing and rearrangements of the optically active (29a) give products with predominant retention of the configuration of the migrating phenylethyl group, but the intramolecular stereoselectivity of the rearrangement is significantly greater than that of the rearrangement.These results are consistent with a radical pair pathway for all three modes of rearrangement.Suitably substituted acyl stabilised allylammonium ylides (55) rearrange by competing , and processes.

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