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1H-Isoindole-1,3(2H)-dione, 2-[[4-(trimethylsilyl)phenyl]methyl]- is a complex organic compound with the molecular formula C18H23NO2Si. It is a derivative of 1H-isoindole-1,3(2H)-dione, featuring a trimethylsilylphenylmethyl group attached to the 2-position. 1H-Isoindole-1,3(2H)-dione, 2-[[4-(trimethylsilyl)phenyl]methyl]- is characterized by its unique structure, which includes a heterocyclic ring system with a carbonyl group at positions 1 and 3, and a silicon-containing aryl group that contributes to its reactivity and stability. It is often used in organic synthesis, particularly in the formation of various pharmaceuticals and other chemical compounds due to its ability to participate in a range of chemical reactions, such as nucleophilic substitutions and condensations.

7662-80-8

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7662-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7662-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,6 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7662-80:
(6*7)+(5*6)+(4*6)+(3*2)+(2*8)+(1*0)=118
118 % 10 = 8
So 7662-80-8 is a valid CAS Registry Number.

7662-80-8Relevant academic research and scientific papers

Analogues of capsaicin with agonist activity as novel analgesic agents: Structure-activity studies. 4. Potent, orally active analgesics

Wrigglesworth, Roger,Walpole, Christopher S. J.,Bevan, Stuart,Campbell, Elizabeth A.,Dray, Andy,Hughes, Glyn A.,James, Iain,Masdin, Kay J.,Winter, Janet

, p. 4942 - 4951 (2007/10/03)

Structural features of three regions of the capsaicin molecule necessary for agonist properties were delineated by a previously reported modular approach. These in vitro agonist effects were shown to correlate with analgesic potency in rodent models. Comb

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