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Cyclohexanol, 1-ethenyl-4-phenyl-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88754-10-3

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88754-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88754-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,5 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88754-10:
(7*8)+(6*8)+(5*7)+(4*5)+(3*4)+(2*1)+(1*0)=173
173 % 10 = 3
So 88754-10-3 is a valid CAS Registry Number.

88754-10-3Relevant academic research and scientific papers

Catalytic Radical-Polar Crossover Reactions of Allylic Alcohols

Touney, Eric E.,Foy, Nicholas J.,Pronin, Sergey V.

supporting information, p. 16982 - 16987 (2018/12/14)

Radical-polar crossover hydrofunctionalizations of tertiary allylic alcohols are described. Depending on the structure of the catalyst, corresponding epoxides or semipinacol rearrangement products are selectively obtained in good yields. Experimental evidence points to the participation of alkylcobalt complexes as electrophilic intermediates.

STEREOSPECIFIC SYNTHESES AND REACTIONS OF ALLYL- AND ALLENYL-SILANES

Fleming, Ian,Terrett, Nicholas K.

, p. 99 - 118 (2007/10/02)

The stereospecifically anti synthesis of allyl- and allenyl-silanes by the reaction of a silylcuprate reagent with allyl and propargyl acetates is described.The SE2' reactions of these silanes with various electrophiles are shown to proceed wit

THE STEREOCHEMISTRY OF SOME SE2' REACTIONS OF ALLYL- AND ALLENYLSILANES

Fleming, Ian,Terrett, Nicholas K.

, p. 4153 - 4156 (2007/10/02)

The SE2' reactions of 1 and 2 with a range of electrophiles are predominantly anti in the allylsilane portion of the molecule, but this offset, to a greater or lesser extent, by axial or equatorial preferences in the ring system.

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