35102-90-0 Usage
Uses
Used in Organic Synthesis:
(4-methoxybenzyl)(dimethyl)silyl is used as a protective group for [alcohol or amine functional groups] in organic synthesis to prevent [unwanted reactions] during the synthesis process.
Used in Pharmaceutical Industry:
(4-methoxybenzyl)(dimethyl)silyl is used as a synthetic intermediate for [creating new pharmaceutical compounds] due to its ability to protect sensitive functional groups and facilitate complex molecular constructions.
Used in Chemical Research:
(4-methoxybenzyl)(dimethyl)silyl is used as a research tool for [exploring new reaction pathways and mechanisms] in the field of synthetic chemistry, providing insights into the reactivity and selectivity of various functional groups.
Used in Material Science:
(4-methoxybenzyl)(dimethyl)silyl is used as a building block for [developing new materials with specific properties], such as those with tailored electronic, optical, or mechanical characteristics, by incorporating this versatile compound into the material's structure.
Check Digit Verification of cas no
The CAS Registry Mumber 35102-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,0 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35102-90:
(7*3)+(6*5)+(5*1)+(4*0)+(3*2)+(2*9)+(1*0)=80
80 % 10 = 0
So 35102-90-0 is a valid CAS Registry Number.
35102-90-0Relevant academic research and scientific papers
Silyl-directed, iridium-catalyzed ortho-borylation of arenes. A one-pot ortho-borylation of phenols, arylamines, and alkylarenes
Boebel, Timothy A.,Hartwig, John F.
, p. 7534 - 7535 (2008/12/22)
The regioselectivity of the borylation of arenes catalyzed by the combination of 4,4′-di-tert-butylbipyridine (dtbpy) and [Ir(cod)Cl]2 has typically been governed by steric effects. We describe a strategy that makes use of a new substituent for ortho-functionalization to overcome this bias. We show that arenes containing hydrosilyl substituents on an atom attached to the arene ring undergo borylation at the position ortho to the hydrosilyl group. Using iridium-catalyzed formation of silyl ethers and silylamines from silanes and either phenols or arylamines, we have developed the ortho-borylation into a one-pot conversion of free phenols and monoprotected anilines into hydroxy- and amino-substituted organoboron derivatives. Copyright
