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Cyclohexanecarbonitrile, 1-[(trimethylsilyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24731-36-0

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24731-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24731-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,3 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24731-36:
(7*2)+(6*4)+(5*7)+(4*3)+(3*1)+(2*3)+(1*6)=100
100 % 10 = 0
So 24731-36-0 is a valid CAS Registry Number.

24731-36-0SDS

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 1-trimethylsilyloxycyclohexane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-trimethylsilyloxy-1-cyclohexanecarbonitrile

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:24731-36-0 SDS

24731-36-0Relevant academic research and scientific papers

Trimethylsilyl cyanide addition to carbonyl compounds under neutral condition catalyzed by iodine

Azizi, Najmedin,Saidi, Mohammad R.

, p. 2111 - 2115 (2003)

Reaction of trimethylsilyl cyanide with aliphatic or aromatic aldehydes and ketones in the presence of a catalytic amount of elemental iodine produced the corresponding cyanohydrin trimethylsilyl ethers in very short time and high yields.

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

Meng, Zhixin,Zhang, Ming,Yang, Hengquan

, p. 627 - 633 (2019)

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

Solvent-free heterogeneous catalysis for cyanosilylation in a modified sodalite-type Cu(II)-MOF

Zhang, Ling-Juan,Han, Cai-Yun,Dang, Qin-Qin,Wang, Yan-Hong,Zhang, Xian-Ming

, p. 24293 - 24298 (2015)

Solvothermal reaction of Cu(OAc)2 and H3BTT·2HCl generated a sodalite-type metal-organic framework [(Cu4O0.27Cl0.73)3(H0.5BTT)8(H2O)12]·3MeOH·9DM

Controllable Synthesis and Catalytic Performance of Nanocrystals of Rare-Earth-Polyoxometalates

Li, Shujun,Zhou, Yanfang,Peng, Qingpo,Wang, Ruoya,Feng, Xiaoge,Liu, Shuxia,Ma, Xiaoming,Ma, Nana,Zhang, Jie,Chang, Yi,Zheng, Zhiping,Chen, Xuenian

, p. 6624 - 6631 (2018)

Large-scale isolation of nanocrystals of rare-earth-polyoxometalates (RE-POMs) catalysts is important in fundamental research and applications. Here, we synthesized a family of monomeric RE-POMs by the self-assembly of Ta/W mixed-addendum POM {P2/su

Determination, par spectrometries infrarouge et Raman, de la stereochimie de cyclohexylcyanhydrines O-trimethylsilylees

Marchand, Annette,Gerval, Pierre,Picard, Jean-Paul

, p. 1735 - 1744 (1991)

A homogeneous series of α-trimethylsiloxynitriles 1-8, obtained by cyanosilylation of cyclohexanones, was investigated by Raman and IR spectroscopies.This study yielded information that complements previous fragmentary NMR results.It was shown that both p

Niobium phytate prepared from phytic acid and NbCl5: A highly efficient and heterogeneous acid catalyst

Xue, Zhimin,Zhang, Yuwei,Li, Guofeng,Wang, Jinfang,Zhao, Wancheng,Mu, Tiancheng

, p. 1070 - 1076 (2016)

The preparation of functional catalysts using naturally-occurring building blocks is of great importance. In this work, we designed a functional heterogeneous acid catalyst, niobium phytate, using phytic acid, which could be obtained from the seeds and grains of plants, as the building block to react with NbCl5. The prepared niobium phytate was characterized by XRD, FT-IR, XPS, SEM, TEM, NH3-TPD and N2 adsorption-desorption examinations. Niobium phytate showed very high activity for both cyanosilylation of carbonyl compounds and dehydration of carbohydrates. It was also found that niobium phytate had higher activity than commercial Nb2O5. In addition, niobium phytate could be easily recovered and reused without reducing the reaction activity considerably. Further study indicated that both higher acidity and lower crystallinity contributed significantly to the excellent catalytic performance of niobium phytate. The findings in this work provide insights into the design of new functional catalysts using naturally-occurring building blocks for various organic reactions.

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

, p. 3809 - 3812 (2020)

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

Supported ionic liquid-like phases as organocatalysts for the solvent-free cyanosilylation of carbonyl compounds: From batch to continuous flow process

Martin, Sergio,Porcar, Raul,Peris, Edgar,Burguete, Maria Isabel,Garcia-Verdugo, Eduardo,Luis, Santiago V.

, p. 1639 - 1647 (2014)

Supported ionic liquid-like phases (SILLPs) are able to efficiently catalyse the cyanosilylation of carbonyl compounds using trimethylsilyl cyanide under solvent-free conditions. These organic catalysts were efficient for various carbonyl compounds includ

Synthesis, characterization, crystal structure of magnesium compound based 3, 3′, 5, 5′-azobenzentetracarboxylic acid and application as high-performance heterogeneous catalyst for cyanosilylation

Li, Yong-Peng,Zhang, Ling-Juan,Ji, Wen-Juan

, p. 607 - 614 (2017)

A novel coordination compound with the formula {[H3O]2[Mg(ABTC)(DMI)2]}n (1) (H4ABTC?=?3,3′,5,5′-azobenzene-tetracarboxylic acid, DMI?=?1,3-dimethy-2-imidazolidinone) as synthesized under solvothermal

Application of an Electrochemical Microflow Reactor for Cyanosilylation: Machine Learning-Assisted Exploration of Suitable Reaction Conditions for Semi-Large-Scale Synthesis

Sato, Eisuke,Fujii, Mayu,Tanaka, Hiroki,Mitsudo, Koichi,Kondo, Masaru,Takizawa, Shinobu,Sasai, Hiroaki,Washio, Takeshi,Ishikawa, Kazunori,Suga, Seiji

supporting information, p. 16035 - 16044 (2021/09/02)

Cyanosilylation of carbonyl compounds provides protected cyanohydrins, which can be converted into many kinds of compounds such as amino alcohols, amides, esters, and carboxylic acids. In particular, the use of trimethylsilyl cyanide as the sole carbon source can avoid the need for more toxic inorganic cyanides. In this paper, we describe an electrochemically initiated cyanosilylation of carbonyl compounds and its application to a microflow reactor. Furthermore, to identify suitable reaction conditions, which reflect considerations beyond simply a high yield, we demonstrate machine learning-assisted optimization. Machine learning can be used to adjust the current and flow rate at the same time and identify the conditions needed to achieve the best productivity.

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