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Silane, trimethyl[(2-nitrophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17876-76-5

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17876-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17876-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17876-76:
(7*1)+(6*7)+(5*8)+(4*7)+(3*6)+(2*7)+(1*6)=155
155 % 10 = 5
So 17876-76-5 is a valid CAS Registry Number.

17876-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[(2-nitrophenyl)methyl]silane

1.2 Other means of identification

Product number -
Other names o-Nitrobenzyltrimethylsilan

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17876-76-5 SDS

17876-76-5Relevant academic research and scientific papers

INDOLE DERIVATIVES, THEIR MANUFACTURE AND USE AS PHARMACEUTICAL AGENTS

-

Page/Page column 25, (2008/06/13)

Objects of the present invention are the compounds of formula I (I), their pharmaceutically acceptable salts, enantiomeric forms, diastereoisomers and racemates, the preparation of the above-mentioned compounds, medicaments containing them and their manuf

Ozone-mediated Nitration of Alkylbenzenes and Related Compounds with Nitrogen Dioxide

Suzuki, Hitomi,Murashima, Takashi,Kozai, Iku,Mori, Tadashi

, p. 1591 - 1598 (2007/10/02)

In the presence of ozone, nitrogen dioxide exhibits a strong nitrating ability for alkylbenzenes at low temperatures, converting them into the corresponding nitro derivatives in high yield.The addition of a protonic acid as catalyst enhances considerably the ability of this nitrating system and leads to a good yield of polynitro compounds.The reaction is clean and proceeds rapidly without any accompanying side-chain substitution or aryl-aryl coupling.It shows no kinetic dependence on the concentration of substrates and, as far as can be judged from relative reactivities and isomer distributions of products, it gives the appearance of being an electrophilic aromatic process.A possible role for nitrogen trioxide has been suggested as the initial electrophilic agent for the nitration of alkylbenzenes.

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