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2-(4-tolyl)-2-(trimethylsiloxy)propanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69813-79-2

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69813-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69813-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,1 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69813-79:
(7*6)+(6*9)+(5*8)+(4*1)+(3*3)+(2*7)+(1*9)=172
172 % 10 = 2
So 69813-79-2 is a valid CAS Registry Number.

69813-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(p-tolyl)-2-((trimethylsilyl)oxy)propanenitrile

1.2 Other means of identification

Product number -
Other names -

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:69813-79-2 SDS

69813-79-2Relevant academic research and scientific papers

n-Butyllithium as a highly efficient precatalyst for cyanosilylation of aldehydes and ketones

Kang, Zihan,Wang, Yuhong,Xu, Xiaojuan,Xue, Mingqiang,Zhang, Wenxuan,Zhou, Shuai,Zhu, Xu

supporting information, p. 7432 - 7437 (2021/09/07)

A highly efficient cyanosilylation protocol mediated by the easily availablen-BuLi with a wide range of aldehydes and ketones was developed. This protocol features excellent yields with very lown-BuLi loadings (0.01-0.05 mol%) at room temperature, solvent

Conjugated Bis-Guanidines (CBGs) as β-Diketimine Analogues: Synthesis, Characterization of CBGs/Their Lithium Salts and CBG Li Catalyzed Addition of B?H and TMSCN to Carbonyls

Peddarao, Thota,Baishya, Ashim,Sarkar, Nabin,Acharya, Rudresh,Nembenna, Sharanappa

, p. 2034 - 2046 (2021/05/27)

Herein, we report a range of conjugated bis-guanidines (CBGs) L [L={(ArHN)(ArHN)C=N?C=(NAr)(NHAr)}; Ar=2, 6-Me2 - C6H3, (1), 2, 4, 6-Me3?C6H2, (2), 2, 6-Et2?C6H3

Synthesis of cyanooxovanadate and cyanosilylation of ketones

Hayashi, Yoshihito,Kawabata, Hiroko,Kikukawa, Yuji

, p. 31688 - 31692 (2021/11/30)

The cyanosilylation was performed by using metavanadate catalysts, and in situ measurements revealed the formation of [VO2(CN)3]2- and [VO4TMS2]- under reaction conditions. The reaction of [VO2(CN)3]2-, trimethylsilyl cyanide (TMSCN), and water afforded [

Nanoceria as a recyclable catalyst/support for the cyanosilylation of ketones and alcohol oxidation in cascade

Garnes-Portolés, Francisco,Leyva-Pérez, Antonio,Rivero-Crespo, Miguel ángel

, p. 21 - 28 (2020/10/21)

The cyanosilylation of carbonyl compounds is a fundamental reaction in organic synthesis, to give cyanohydrins. Ketones are particularly reluctant to cyanosilane addition and require the action of a catalyst, and despite many soluble Br?nsted and Lewis ac

A micro-environment tuning approach for enhancing the catalytic capabilities of lanthanide containing polyoxometalate in the cyanosilylation of ketones

Li, Sang-Hao,Lin, Ming-Yuan,Nie, Yan-Mei,Yan, Jun

supporting information, p. 3809 - 3812 (2020/04/10)

The as-synthesized (TBA)8H5[Nd(SiW11O39)2] manifested high catalytic activity for cyanosilylation of ketones, and its catalytic activity could be improved further through rational design of the reacti

Application of n-butyllithium in catalyzing cyanosilylation reaction of ketone and silane

-

Paragraph 0024, (2020/07/13)

The invention discloses an application of n-butyllithium in catalyzing cyanosilylation reaction of ketone and silane. The n-butyllithium has high catalytic activity, low catalyst dosage and good substrate application range. After n-butyllithium, ketone an

Pickering emulsion droplets hosting ionic liquid catalysts for continuous-flow cyanosilylation reaction

Meng, Zhixin,Zhang, Ming,Yang, Hengquan

, p. 627 - 633 (2019/02/14)

An IL-catalyzed cyanosilylation reaction is an important route for synthesis of many fine chemicals, but it is currently conducted in a batch manner. Herein, we have developed a novel method to "immobilize" IL catalysts for continuous-flow reaction based

Syntheses, Structures, and Catalytic Activities of the Anionic Heterobimetallic Rare-Earth Metal Complexes Supported by Pyrrolyl-Substituted 1,2-Diimino Ligands

Wang, Wei,Wang, Xiaojia,Zhou, Shuangliu,Xu, Xiaolong,Du, Jun,Zhang, Lijun,Mu, Xiaolong,Wei, Yun,Zhu, Xiancui,Wang, Shaowu

supporting information, p. 10390 - 10400 (2018/08/28)

A series of the anionic heterobimetallic rare-earth metal complexes supported by trans- or chiral pyrrolyl-substituted 1,2-diimino ligands were synthesized in good yields via reactions of [(Me3Si)2N]3RE(μ-Cl)Li(THF)3

Cyanosilylation reaction method using hydroboron to catalyze ketone

-

Paragraph 0033, (2018/05/03)

The invention relates to the field of organic chemistry, aiming at solving the problems that the existing ketone-catalyzing cyanosilylation reaction has the defects of complicated catalyst structure,high preparation cost and more application limitations,

Beyond Hydrofunctionalisation: A Well-Defined Calcium Compound Catalysed Mild and Efficient Carbonyl Cyanosilylation

Yadav, Sandeep,Dixit, Ruchi,Vanka, Kumar,Sen, Sakya S.

supporting information, p. 1269 - 1273 (2018/02/06)

Organocalcium compounds have been reported as efficient catalysts for various transformations, for cases in which one of the substrates contained an E?H (E=B, N, Si, P) bond. Here, we look at the possibility of employing an organocalcium compound for a tr

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