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α-methallyldiphenylmethylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108733-51-3

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108733-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108733-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,3 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108733-51:
(8*1)+(7*0)+(6*8)+(5*7)+(4*3)+(3*3)+(2*5)+(1*1)=123
123 % 10 = 3
So 108733-51-3 is a valid CAS Registry Number.

108733-51-3Downstream Products

108733-51-3Relevant academic research and scientific papers

Free radical addition to branched allylsilanes: Stereoselective formation and elimination of β bromosilanes

Porter, Ned A.,Zhang, Guiru,Reed, Aimee D.

, p. 5773 - 5777 (2000)

Lewis acid-promoted free radical addition to 3-silyl-1-butenes occurs in good yield to give predominantly the cis-substituted alkene. The transfer reaction occurs by atom-transfer addition of the alkyl bromide precursor, an addition that occurs by Felkin-

SELECTIVE SYNTHESIS OF (E)-CROTYLSILANES BY REACTION OF CROTYLMAGNESIUM BROMIDE WITH HYDROSILANES IN THE PRESENCE OF DICHLORONIKKEL(II)

Hayashi, Tamio,Kabeta, Keiji,Kumada, Makoto

, p. 1499 - 1500 (1984)

Dichloronickel(II) was found to be an effective catalyst for the reaction of crotylmagnesium bromide with hydrosilanes to give (E)-crotyl-silanes selectively.

Regioselective Carboxylation of Silicon-Stabilized Allylic Carbanions and the Synthetic Utility of 2-Silyl-3-butenoates

Uno, Hidemitsu

, p. 2471 - 2480 (2007/10/02)

Carbanions of allylic dimethylphenylsilanes show remarkable regioselectivity toward carboxylation with carbon dioxide and methylation with methyl iodide.Methylationn of these compounds occurred preferentially at α position, although allyltrimethylsilane and allyltriphenylsilane are known to give γ selectivity toward the same electrophiles.Moreover, their aluminum "ate" complexes react with carbon dioxide regioselectively at the α position irrespective of methyl substitution pattern of the allylic moieties.The α-carboxylated allylic silanes proved to be useful synthons of 3-(methoxycarbonyl)allyl anions after esterifiaction.

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