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2-(4-(trifluoromethyl)phenyl)-2-((trimethylsilyl)oxy)acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73183-23-0 Structure
  • Basic information

    1. Product Name: 2-(4-(trifluoromethyl)phenyl)-2-((trimethylsilyl)oxy)acetonitrile
    2. Synonyms: 2-(4-(trifluoromethyl)phenyl)-2-((trimethylsilyl)oxy)acetonitrile
    3. CAS NO:73183-23-0
    4. Molecular Formula:
    5. Molecular Weight: 273.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73183-23-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4-(trifluoromethyl)phenyl)-2-((trimethylsilyl)oxy)acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-(trifluoromethyl)phenyl)-2-((trimethylsilyl)oxy)acetonitrile(73183-23-0)
    11. EPA Substance Registry System: 2-(4-(trifluoromethyl)phenyl)-2-((trimethylsilyl)oxy)acetonitrile(73183-23-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 73183-23-0(Hazardous Substances Data)

73183-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73183-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73183-23:
(7*7)+(6*3)+(5*1)+(4*8)+(3*3)+(2*2)+(1*3)=120
120 % 10 = 0
So 73183-23-0 is a valid CAS Registry Number.

73183-23-0Relevant articles and documents

Role of metal center and coordination environment in M-(Z)-N-((E)-pyridin-2-ylmethylene)isonicotinohydrazonate (M = LaIII, ZnII, CdII or HgII) catalyzed cyanosilylation of aldehydes

Hajiyeva, Sevinc R.,Huseynov, Fatali E.,Kopylovich, Maximilian N.,Mahmoudi, Ghodrat,Nikitina, Eugeniya V.,Prisyazhnyuk, Ekaterina D.,Shamilov, Nazim T.,Zubkov, Fedor I.

, (2021/09/07)

A series of known metal complexes, [LaL2(NO3)(H2O)2]·5H2O (1), [Zn(μ-L)(NO3)(H2O)]n (2), {[Cd2(μ-HL)(μ-L)(NO3)3(H2O)]·Hsub

Silyl Cyanopalladate-Catalyzed Friedel-Crafts-Type Cyclization Affording 3-Aryloxindole Derivatives

Ece, Hamdiye,Tange, Yuji,Yurino, Taiga,Ohkuma, Takeshi

supporting information, p. 935 - 939 (2021/02/22)

3-Aryloxindole derivatives were synthesized through a Friedel-Crafts-type cyclization. The reaction was catalyzed by a trimethylsilyl tricyanopalladate complex generated in situ from trimethylsilyl cyanide and Pd(OAc) 2. Wide varieties of diethyl phosphates derived from N -arylmandelamides were converted almost quantitatively into oxindoles. When N, N -dibenzylamide was used instead of an anilide substrate, a benzo-fused δ-lactam was obtained. An oxindole product was subjected to substitution reactions to afford 3,3-diaryloxindoles with two different aryl groups.

Constructing a triangular metallacycle with salen-Al and its application to a catalytic cyanosilylation reaction

Li, Bo,Li, Yang,Qiu, Huayu,Xu, Jun,Yin, Shouchun,Zhang, Jinjin,Zhang, Pengfei,Zhang, Yueyue

supporting information, p. 10399 - 10402 (2021/10/12)

A triangular metallosalen-based metallacycle was constructed in quantitative yield by the self-assembly of a 180° bis(pyridyl)salen-Al complex and a 60° diplatinum(ii) acceptor in a 1?:?1 stoichiometric ratio. This metallacycle was then successfully used to cyanosilylate a wide range of benzaldehydes with trimethylsilyl cyanide.

The direct trifluoromethylsilylation and cyanosilylation of aldehydes: via an electrochemically induced intramolecular pathway

Yang, Hui,Shen, Yongli,Xiao, Zihui,Liu, Caiyan,Yuan, Kedong,Ding, Yi

supporting information, p. 2435 - 2438 (2020/03/06)

The initiator-free electrochemical trifluoromethylsilylation and cyanosilylation of aldehydes were developed in an undivided cell. A DFT study reveals that the direct cathodic activation of trimethylsilyl reagents significantly released the congestion around the 'Si' atom, allowing the Si-O bond affinity to form concerted anion intermediates with aldehydes. Thus, intramolecular -CF3 and -CN migration make the reactions much easier to carry out without initiators.

Tunable morphology and the changeable catalytic property of layered scandium coordination polymer

Zhu, Ziqian,Tong, Chengxia,Wang, Pengcheng,Wang, Wei,Sun, Jing,Xue, Jingjing,Wang, Li,Fan, Yong,Xu, Jianing

, (2020/01/08)

Sc-CP 1, 1A, 1B and 1C with controllable morphologies were successfully synthesized by the conventional hydrothermal method and microwave (MW) assisted hydrothermal method. 1 was macroscopic, 1A was nano sized, while 1B and 1C were micron sized. Sc-CP 1 s

Discovery of the First in Vivo Active Inhibitors of the Soluble Epoxide Hydrolase Phosphatase Domain

Kramer, Jan S.,Woltersdorf, Stefano,Duflot, Thomas,Hiesinger, Kerstin,Lillich, Felix F.,Kn?ll, Felix,Wittmann, Sandra K.,Klingler, Franca-M.,Brunst, Steffen,Chaikuad, Apirat,Morisseau, Christophe,Hammock, Bruce D.,Buccellati, Carola,Sala, Angelo,Rovati, G. Enrico,Leuillier, Matthieu,Fraineau, Sylvain,Rondeaux, Julie,Hernandez-Olmos, Victor,Heering, Jan,Merk, Daniel,Pogoryelov, Denys,Steinhilber, Dieter,Knapp, Stefan,Bellien, Jeremy,Proschak, Ewgenij

, p. 8443 - 8460 (2019/10/16)

The emerging pharmacological target soluble epoxide hydrolase (sEH) is a bifunctional enzyme exhibiting two different catalytic activities that are located in two distinct domains. Although the physiological role of the C-terminal hydrolase domain is well-investigated, little is known about its phosphatase activity, located in the N-terminal phosphatase domain of sEH (sEH-P). Herein we report the discovery and optimization of the first inhibitor of human and rat sEH-P that is applicable in vivo. X-ray structure analysis of the sEH phosphatase domain complexed with an inhibitor provides insights in the molecular basis of small-molecule sEH-P inhibition and helps to rationalize the structure-activity relationships. 4-(4-(3,4-Dichlorophenyl)-5-phenyloxazol-2-yl)butanoic acid (22b, SWE101) has an excellent pharmacokinetic and pharmacodynamic profile in rats and enables the investigation of the physiological and pathophysiological role of sEH-P in vivo.

PhI(OAc)2-mediated alkoxyoxygenation of β,γ-unsaturated ketoximes: Preparation of isoxazolines bearing two contiguous tetrasubstituted carbons

Ye, Chenghao,Kou, Xuezhen,Yang, Guoqiang,Shen, Jiefeng,Zhang, Wanbin

supporting information, p. 1148 - 1152 (2019/03/26)

A PhI(OAc)2-promoted dioxygenation of allyl oximes, including one alkoxylation, has been developed. This reaction can give isoxazoline products bearing two contiguous tetrasubstituted carbons. Various oximes substrates bearing different aryl groups and tetrasubstituted-olefin moieties were compatible with the mild reaction conditions. A two-electron oxidation pathway was proposed based on results of preliminary mechanistic studies.

Two scandium coordination polymers: Rapid synthesis and catalytic properties

Zhu, Ziqian,Tao, Yufang,Jiang, Yansong,Zhang, Liying,Xu, Jianing,Wang, Li,Fan, Yong

, p. 5261 - 5268 (2019/09/16)

Two scandium coordination polymers (Sc-CPs), [Sc(L1)2(DMF)] (DMF = N,N′-dimethyl formamide, H2L1 = pyrazine-2,3-dicarboxylic acid) (1) and [Sc(L2)(C2O4)0.5(H2/su

Dimeric alumatranes as catalysts for trimethylsilylcyanation reaction

Kim, Yoseph,Lee, Kang Mun,Kim, So Han,Moon, Jung Hee,Kim, Youngjo

, p. 48151 - 48160 (2017/11/03)

The solid-state structures of dimeric alumatranes with three five-membered rings chelated by [(OCMe2CH2)nN(CH2CH2O)3-n]3- (n = 1, L1; n = 2, L2; n = 3, L3), which vary by the num

Insight into the catalytic properties and applications of metal-organic frameworks in the cyanosilylation of aldehydes

Zhang, Zhiguo,Chen, Jingwen,Bao, Zongbi,Chang, Ganggang,Xing, Huabin,Ren, Qilong

, p. 79355 - 79360 (2015/10/05)

Here we present a systematic investigation of the cyanosilylation of aldehydes with trimethylsilyl cyanide (TMSCN) by using metal-organic frameworks (MOFs) as catalysts. Four types of thermally stable MOFs (MIL-47 (V), MIL-53 (Al), MIL-101 (Cr), and UiO-6

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