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CAS

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51667-07-3

Silane, trimethyl(4-phenyl-1,3-butadienyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 51667-07-3 Structure

  • Basic information

    1. Product Name: Silane, trimethyl(4-phenyl-1,3-butadienyl)-
    2. Synonyms:
    3. CAS NO:51667-07-3
    4. Molecular Formula: C13H18Si
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 51667-07-3.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: Silane, trimethyl(4-phenyl-1,3-butadienyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, trimethyl(4-phenyl-1,3-butadienyl)-(51667-07-3)
    11. EPA Substance Registry System: Silane, trimethyl(4-phenyl-1,3-butadienyl)-(51667-07-3)

  • 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: 51667-07-3(Hazardous Substances Data)

51667-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51667-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,6 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51667-07:
(7*5)+(6*1)+(5*6)+(4*6)+(3*7)+(2*0)+(1*7)=123
123 % 10 = 3
So 51667-07-3 is a valid CAS Registry Number.

51667-07-3Relevant articles and documents

LE BIS(TRIMETHYLSILYL)-1,3-PROPENE COMME PRECURSEURS DES SILYL-1-BUTADIENES; ETUDE DE LEUR COMPLEXATION PAR Fe(CO)5, Fe2(CO)9, ET (MeCp)Mn(CO)3

Corriu, R.,Escudie, N.,Guerin, C.

, p. 207 - 216 (1984)

Reactions of 1,3-bis(trimethylsilyl)propene with carbonyl compounds in the presence of fluoride ions as catalysts, produce selectively (E)-1-trimethylsilylbut-1-en-4-ol. 1,3-Bis(trimethylsilyl)propenyllithium reacts with carbonyl compounds, under formatio

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