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62269-21-0

2-Propenenitrile, 3-phenyl-3-[(trimethylsilyl)oxy]-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 62269-21-0 Structure

  • Basic information

    1. Product Name: 2-Propenenitrile, 3-phenyl-3-[(trimethylsilyl)oxy]-, (Z)-
    2. Synonyms:
    3. CAS NO:62269-21-0
    4. Molecular Formula: C12H15NOSi
    5. Molecular Weight: 217.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 62269-21-0.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-Propenenitrile, 3-phenyl-3-[(trimethylsilyl)oxy]-, (Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Propenenitrile, 3-phenyl-3-[(trimethylsilyl)oxy]-, (Z)-(62269-21-0)
    11. EPA Substance Registry System: 2-Propenenitrile, 3-phenyl-3-[(trimethylsilyl)oxy]-, (Z)-(62269-21-0)

  • 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: 62269-21-0(Hazardous Substances Data)

62269-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62269-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,6 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62269-21:
(7*6)+(6*2)+(5*2)+(4*6)+(3*9)+(2*2)+(1*1)=120
120 % 10 = 0
So 62269-21-0 is a valid CAS Registry Number.

62269-21-0Relevant articles and documents

Stereocontrolled conversion of 3-unsubstituted isoxazole compounds into Z-β-siloxyacrylonitriles. A new method for the regioselective synthesis of β-enaminoketones

Gonzalez,Gonzalez,Pulido

, p. 1005 - 1014 (2007/10/02)

The stereoselective synthesis of Z-β-siloxyacrylonitriles via base-induced ring cleavage of isoxazole precursors is described. Z-β-siloxyacrylonitriles react with organolithium compounds to give high yields of β-enaminoketones 1.

SYNTHESIS OF Z-β-SILOXYACRYLONITRILES AND STUDY OF THEIR DIENOPHILIC PROPERTIES

Alberola, A.,Gonzalez, A. M.,Gonzalez, B.,Laguna, M. A.,Pulido, F. J.

, p. 2027 - 2030 (2007/10/02)

A general method for the synthesis of Z-β-siloxyacrylonitriles from isoxazoles is reported.Their dienophilic activity is also described.

SYNTHESIS AND REARRANGEMENT OF CYCLOADDUCTS FROM TRIMETHYLSILANECARBONITRILE OXIDE

Sarlo, Francesco De,Brandi, Alberto,Goti, Andrea,Guarna, Antonio,Rovero, Paolo

, p. 511 - 518 (2007/10/02)

The cycloadducts from trimethylsilanecarbonitrile oxide and ethylenic or acetylenic compounds easily rearrange to open-chain intermediates, which, in turn, are hydrolysed respectively to β-hydroxynitriles and β-oxonitriles.The cycloadducts of the same nitrile oxide with sulfur dioxide and sulfinylamines are unstable, too, leading respectively to trimethylsilylisocyanate and trimethylsilylcarbodiimides.All these reactions are of preparative interest, in comparison with previous methods.

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