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25438-37-3

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25438-37-3 Usage

General Description

ALPHA-(TRIMETHYLSILYLOXY)PHENYLACETONITRILE is a chemical compound with the molecular formula C11H15NOSi, which is used as a building block in the synthesis of various organic compounds. It is a nitrile derivative with a trimethylsilyloxy group attached to the phenylacetone moiety. ALPHA-(TRIMETHYLSILYLOXY)PHENYLACETONIT& is commonly used in the pharmaceutical and agrochemical industries for the production of drugs and pesticides. It is known for its ability to undergo various chemical reactions, making it a versatile compound in organic synthesis. Additionally, it is often used as a reactant in the preparation of complex molecular structures due to its stability and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 25438-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,3 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25438-37:
(7*2)+(6*5)+(5*4)+(4*3)+(3*8)+(2*3)+(1*7)=113
113 % 10 = 3
So 25438-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NOSi/c1-14(2,3)13-11(9-12)10-7-5-4-6-8-10/h4-8,11H,1-3H3

25438-37-3SDS

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-phenyl-2-trimethylsilyloxyacetonitrile

1.2 Other means of identification

Product number -
Other names Phenyl-trimethylsilanyloxy-acetonitrile

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:25438-37-3 SDS

25438-37-3Relevant articles and documents

Syntheses, structures, molecular and cationic recognitions and catalytic properties of two lanthanide coordination polymers based on a flexible tricarboxylate

Zhu, Yu,Wang, Yan-Mei,Xu, Ji,Liu, Pan,Weththasinha,Wu, Yun-Long,Lu, Xiao-Qing,Xie, Ji-Min

, p. 259 - 264 (2014)

Two lanthanide coordination polymers, namely, {[La(TTTA)(H 2O)2]·2H2O}n (La-TTTA) and [Nd(TTTA)(H2O)2]·2H2O}n (Nd-TTTA) have been hydrothermally synthesized through th

Bifunctional 2D Cd(II)-Based Metal-Organic Framework as Efficient Heterogeneous Catalyst for the Formation of C-C Bond

Hu, Lei,Hao, Gui-Xia,Luo, Hai-Dong,Ke, Chun-Xian,Shi, Guang,Lin, Jia,Lin, Xiao-Ming,Qazi, Umair Yaqub,Cai, Yue-Peng

, p. 2883 - 2889 (2018)

A porous two-dimensional (2D) metal-organic framework (MOF), namely, [Cd(PBA)(DMF)]·DMF (Cd-PBA), has been solvothermally synthesized by the reaction of 5-(4-pyridin-3-yl-benzoylamino)-isophthalic acid ligand (H2PBA) and Cd(II) ions. Structural

Hollow silica nanosphere having functionalized interior surface with thin manganese oxide layer: Nanoreactor framework for size-selective Lewis acid catalysis

Anisur, Rahman Md,Shin, Jongmin,Choi, Hyung Ho,Yeo, Kyung Min,Kang, Eun Joo,Lee, In Su

, p. 10615 - 10621 (2010)

A novel selective nanoscale etching process that generated a well defined hollow nanostructure was developed by treating manganese oxide nanoparticles with a hydroxylamine solution. This selective etching process was used for exploiting a novel method of differentially functionalizing the internal surface of a hollow silica shell with a catalytically active Mn3O 4 layer and creating a novel nanoreactor framework. The nanoreactor fabricated by the newly developed method catalyzed the cyanosilylation reactions of various aromatic aldehydes with size and shape selectivity. Moreover, the substrate selectivity in the cyanosilylation reactions was efficiently tuned by modifying the outer silica shell with silane coupling reagents.

Syntheses, structures and catalytic properties of organic-inorganic hybrid materials constructed from Evans-Showell-type polyoxometalates and zinc-organic coordination units

Fei, Fei,An, Haiyan,Xu, Tieqi,Meng, Changgong

, p. 92092 - 92103 (2016)

Four new organic-inorganic hybrid compounds based on the polyoxoanion [Co2Mo10H4O38]6-, namely [Zn2(H2O)5(4,4′-bipy)3]H2[Co2Mo10

Improving the porosity and catalytic capacity of a zinc paddlewheel metal-organic framework (MOF) through metal-ion metathesis in a single-crystal-to-single-crystal fashion

Yang, Jie,Wang, Xiaoqing,Dai, Fangna,Zhang, Liangliang,Wang, Rongming,Sun, Daofeng

, p. 10649 - 10653 (2014)

Zinc paddlewheel metal-organic frameworks (MOFs) frequently exhibit low stability or complete collapse upon the removal of axial ligands. Hence, there are very few reports on gas adsorption of zinc paddlewheel MOFs. In this work, the N2 and Hs

Lanthanide-Based Metal-Organic Frameworks Containing "v-Shaped" Tetracarboxylate Ligands: Synthesis, Crystal Structures, "naked-Eye" Luminescent Detection, and Catalytic Properties

Wu, Pengyan,Xia, Lingling,Huangfu, Mengjie,Fu, Fubin,Wang, Mengqiu,Wen, Bingxin,Yang, Ziyun,Wang, Jian

, p. 264 - 273 (2020)

Three lanthanide-based metal-organic frameworks, [Tb(HMDIA)(H2O)3]·H2O (Tb-MDIA), [Ho(HMDIA)(H2O)3]·(H2O)2 (Ho-MDIA), and [Nd(HMDIA)(H2O)3]·(H2O)

O,N-Heterocyclic germylenes as efficient catalysts for hydroboration and cyanosilylation of benzaldehyde

Arsenyeva, Kseniya V.,Pashanova, Kira I.,Trofimova, Olesya Yu.,Ershova, Irina V.,Chegerev, Maxim G.,Starikova, Alyona A.,Cherkasov, Anton V.,Syroeshkin, Mikhail A.,Kozmenkova, Anna Ya.,Piskunov, Alexandr V.

, p. 11758 - 11767 (2021/07/12)

New monomeric O,N-heterocyclic germylene AdAPGe (1) based on 4,6-di-tert-butyl-N-adamantyl-o-aminophenol is synthesized and structurally characterized. Germylene 1 in the crystal demonstrates weak Ge?Ge interactions between adjacent molecules. The redox activity of compound 1 and its known analogs PhAPGe (2), t-BuAPGe (3) was studied using cyclic voltammetry and chemical oxidation by the phenoxy radical. Germylene 1, as opposed to 2 and 3, was found to form a relatively stable o-iminosemiquinonate moiety during oxidation. The last one was detected by EPR spectroscopy in toluene solution at low temperatures. The catalytic activity of germylenes 1-3 and dippAPGe (4) (dipp-2,6-di-isopropylphenyl) towards hydroboration and cyanosilylation of benzaldehyde was examined. Germylene 1 demonstrates the most potent promoter properties for such reactions, which allowed cyanosilylation and hydroboration of aldehyde under mild conditions with excellent conversion quickly. Theoretical studies were performed to establish the mechanism, and different reaction routes were examined. According to the DFT (B3LYP/def2-SVP) calculation, cyanosilylation and hydroboration processes are initiated by coordinating TMSCN or HBpin with the catalyst. The followed reaction with aldehyde leads to the resulting products.

Valmet Chiral Schiff-Base Ligands And Their Copper(II) Complexes as Organo, Homogeneous and Heterogeneous Catalysts for Henry, Cyanosilylation and Aldol Coupling Reactions

Arora, Zinnia,Eftemie, Diana-Ioana,Spinciu, Adela,Maxim, C?t?lin,Hanganu, Ana-Maria,Tudorache, Madalina,Cojocaru, Bogdan,Pavel, Octavian D.,Granger, Pascal,Andruh, Marius,Parvulescu, Vasile I.

, p. 4634 - 4644 (2021/09/08)

Cyanosilylation, aldol coupling and asymmetric Henry reactions were carried out with L- and D-valmet ligands in different configurations: i) coordinated to sodium ions, as organocatalysts, with week base properties, ii) complexes with copper(II), as homogeneous catalysts, and iii) immobilized copper(II) complexes onto graphene oxide (GO) as heterogeneous catalysts. For the reaction of benzaldehyde and nitromethane in water these afforded an asymmetric Henry reaction, with a spectacular increase of the conversion and ee (92.5 and 95.8 %, respectively) after the deposition on GO. Ligand complexed copper was also effective for cyanosilylation and Aldol coupling reaction.

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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