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121730-97-0

ethyl 4,4-diphenyl-2-isopropyl-3-butenoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121730-97-0 Structure

  • Basic information

    1. Product Name: ethyl 4,4-diphenyl-2-isopropyl-3-butenoate
    2. Synonyms: ethyl 4,4-diphenyl-2-isopropyl-3-butenoate
    3. CAS NO:121730-97-0
    4. Molecular Formula:
    5. Molecular Weight: 308.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121730-97-0.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: ethyl 4,4-diphenyl-2-isopropyl-3-butenoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 4,4-diphenyl-2-isopropyl-3-butenoate(121730-97-0)
    11. EPA Substance Registry System: ethyl 4,4-diphenyl-2-isopropyl-3-butenoate(121730-97-0)

  • 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: 121730-97-0(Hazardous Substances Data)

121730-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121730-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,7,3 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121730-97:
(8*1)+(7*2)+(6*1)+(5*7)+(4*3)+(3*0)+(2*9)+(1*7)=100
100 % 10 = 0
So 121730-97-0 is a valid CAS Registry Number.

121730-97-0Relevant articles and documents

Unusual Rearrangements in Di-?-methane Systems: Mechanistic and Exploratory Organic Photochemistry

Zimmerman, Howard E.,Cassel, Jonathan M.

, p. 3800 - 3816 (1989)

The triplet photochemistry of 1,1-dicyano-5,5-diphenyl-3,3-diisopropyl-1,4-pentadiene was investigated to determine if the high reactivity of di-?-methane systems with central diphenyl substitution derived from electronic or from steric effects.Sensitized

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