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Benzeneacetonitrile, a-ethyl-a-[(trimethylsilyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75072-04-7

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75072-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75072-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75072-04:
(7*7)+(6*5)+(5*0)+(4*7)+(3*2)+(2*0)+(1*4)=117
117 % 10 = 7
So 75072-04-7 is a valid CAS Registry Number.

75072-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(trimethylsilyloxy)-2-phenylbutanenitrile

1.2 Other means of identification

Product number -
Other names 2-Phenyl-2-trimethylsilanyloxy-butyronitrile

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:75072-04-7 SDS

75072-04-7Relevant academic research and scientific papers

A family of highly stable lanthanide metal-organic frameworks: Structural evolution and catalytic activity

Gustafsson, Mikaela,Bartoszewicz, Agnieszka,Martiin-Matute, Belein,Sun, Junliang,Grins, Jekabs,Zhao, Tony,Li, Zhongyue,Zhu, Guangshan,Zou, Xiaodong

, p. 3316 - 3322 (2010)

A family of homeotypic porous lanthanide metal-organic frameworks (MOFs), [Ln(btc)(H2O)]·guest (Nd (1), Sm (2), Eu (3), Gd (4), Tb (5), Ho (6), Er (7), and Yb (8); guest: DMF or H2O) was synthesized. The structures of the as-synthesi

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 [

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

Meng, Zhixin,Zhang, Ming,Yang, Hengquan

supporting information, 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

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

Lewis Acid Rather than Bronsted Acid Sites of Montmorillonite K10 Act as a Powerful and Reusable Green Heterogeneous Catalyst for Rapid Cyanosilylation of Ketones

Huang, Xiao,Chen, Lin,Ren, Fengying,Yang, Chen,Li, Jianghong,Shi, Kejin,Gou, Xiaojun,Wang, Wei

, p. 439 - 444 (2017/02/24)

A practical green protocol was developed for highly efficient cyanosilylation of various ketones catalyzed by commercial montmorillonite K10, with excellent isolated yields (91-99%). The catalyst can be used as received, and its catalytic strength can be

Porous barium-organic frameworks with highly efficient catalytic capacity and fluorescence sensing ability

Liu, Fuling,Xu, Yuwen,Zhao, Lianming,Zhang, Liangliang,Guo, Wenyue,Wang, Rongming,Sun, Daofeng

supporting information, p. 21545 - 21552 (2015/11/10)

The current study describes the first barium-organic framework with permanent porosity, efficient catalytic capacity, and highly selective luminescence sensing of DMSO molecules and metal ions. Single-crystal-to-single-crystal transformations (from comple

Efficient, rapid and solvent-free cyanosilylation of aldehydes and ketones catalyzed by SbCl3

Pourmousavi,Salahshornia

experimental part, p. 1575 - 1578 (2011/12/15)

Antimony trichloride(SbCl3) was demonstrated to be an effective catalyst for the cyanosilylation of a wide variety of carbonyl compounds under solvent-free conditions. The reactions proceeded smoothly at room temperature to afford the correspon

A dream combination for catalysis: Highly reactive and recyclable scandium(iii) triflate-catalyzed cyanosilylations of carbonyl compounds in an ionic liquid

Park, Boyoung Y.,Ryu, Ka Yeon,Park, Jung Hwan,Lee, Sang-Gi

experimental part, p. 946 - 948 (2010/04/23)

The catalytic activity of lanthanide triflates, particularly scandium triflate, increased dramatically in [bmim][SbF6], allowing the cyanosilylation of a variety of aldehydes and ketones with a turnover frequency up to 48000 mol h-1 and a total turnover number of 100000.

Highly efficient cyanosilylation of sterically bulky ketones catalyzed by tin ion-exchanged montmorillonite

Wang, Jiacheng,Masui, Yoichi,Watanabe, Kenya,Onaka, Makoto

supporting information; experimental part, p. 553 - 557 (2009/10/25)

Tin ion-exchanged montmorillonite (SnMont) was found to be a powerful catalyst for the cyanosilylation of aromatic and aliphatic ketones having a carbonyl group in sterically congested circumstances with cyanotrimethylsilane, giving the corresponding cyan

Tris(2,4,6-trimethoxyphenyl)phosphine (TTMPP): Efficient catalysts for the cyanosilylation and cyanocarbonation of aldehydes and ketones

Matsukawa, Satoru,Sekine, Izumi,Iitsuka, Ayumi

experimental part, p. 3353 - 3359 (2009/12/26)

A variety of aldehydes and ketones were transformed to their corresponding cyanohydrin silyl ethers in good to excellent yields in the presence of 1-5 mol% of tris(2,4,6-trimethoxyphenyl)phosphine (TTMPP). Cyanohydrin carbonates were also readily prepared using 5-10 mol% of TTMPP as an organocatalyst.

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