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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 articles and documents

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.

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

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

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

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

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

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 [

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