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761401-96-1

3E-(methyldiphenylsilyl)-2-propenal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 761401-96-1 Structure

  • Basic information

    1. Product Name: 3E-(methyldiphenylsilyl)-2-propenal
    2. Synonyms: 3E-(methyldiphenylsilyl)-2-propenal
    3. CAS NO:761401-96-1
    4. Molecular Formula:
    5. Molecular Weight: 252.388
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 761401-96-1.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: 3E-(methyldiphenylsilyl)-2-propenal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3E-(methyldiphenylsilyl)-2-propenal(761401-96-1)
    11. EPA Substance Registry System: 3E-(methyldiphenylsilyl)-2-propenal(761401-96-1)

  • 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: 761401-96-1(Hazardous Substances Data)

761401-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 761401-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,4,0 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 761401-96:
(8*7)+(7*6)+(6*1)+(5*4)+(4*0)+(3*1)+(2*9)+(1*6)=151
151 % 10 = 1
So 761401-96-1 is a valid CAS Registry Number.

761401-96-1Relevant articles and documents

Directed ring-closing metathesis of trienes by silyl substitution

Schultz-Fademrecht, Carsten,Deshmukh, Prashant H.,Malagu, Karine,Procopiou, Panayiotis A.,Barrett, Anthony G.M.

, p. 7515 - 7524 (2007/10/03)

A synthetic strategy for 'disarming' a terminal alkene by substitution with a bulky silyl blocking group has been developed. In a series of model studies, sequential selective ring-closing metathesis of trienes followed by selective mono-hydrogenation of the resulting diene is described. The bulky silylated alkene is activated for a subsequent cross-metathesis reaction with a range of diverse alkenes by protodesilylation.

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