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Trimethyl{4-[(trimethylsilyl)oxy]phenyl}silane is an organosilicon compound with the molecular formula C12H21OSi2. It features a trimethylsilyl group (Si(CH3)3) attached to a phenyl ring, which in turn is connected to another trimethylsilyl group through an oxygen atom. trimethyl{4-[(trimethylsilyl)oxy]phenyl}silane is characterized by its symmetrical structure and the presence of two trimethylsilyl groups, which contribute to its unique chemical properties. It is often used in organic synthesis, particularly in the formation of silyl ethers and as a protecting group in various chemical reactions. The compound's stability and reactivity make it a valuable intermediate in the synthesis of more complex organosilicon molecules.

18036-81-2

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18036-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18036-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,3 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18036-81:
(7*1)+(6*8)+(5*0)+(4*3)+(3*6)+(2*8)+(1*1)=102
102 % 10 = 2
So 18036-81-2 is a valid CAS Registry Number.

18036-81-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-(4-trimethylsilyloxyphenyl)silane

1.2 Other means of identification

Product number -
Other names Trimethyl-<p-trimethylsilyl-phenoxy>-silan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:18036-81-2 SDS

18036-81-2Relevant academic research and scientific papers

Synthetic equivalents of benzenethiol and benzyl mercaptan having faint smell: Odor reducing effect of trialkylsilyl group

Nishide, Kiyoharu,Miyamoto, Tetsuo,Kumar, Kamal,Ohsugi, Shin-Ichi,Node, Manabu

, p. 8569 - 8573 (2007/10/03)

Syntheses and odor tests of the trialkylsilylated benzyl mercaptans and benzenethiols have revealed that the trimethylsilyl substituent on the benzene ring has a remarkable effect in reducing the foul smell of the parent benzyl mercaptan and benzenethiol.

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