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CAS

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1219827-88-9

3-ethyl-3-phenylhex-4-enal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1219827-88-9 Structure

  • Basic information

    1. Product Name: 3-ethyl-3-phenylhex-4-enal
    2. Synonyms:
    3. CAS NO:1219827-88-9
    4. Molecular Formula:
    5. Molecular Weight: 202.296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1219827-88-9.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: 3-ethyl-3-phenylhex-4-enal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-ethyl-3-phenylhex-4-enal(1219827-88-9)
    11. EPA Substance Registry System: 3-ethyl-3-phenylhex-4-enal(1219827-88-9)

  • 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: 1219827-88-9(Hazardous Substances Data)

1219827-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1219827-88-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,8,2 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1219827-88:
(9*1)+(8*2)+(7*1)+(6*9)+(5*8)+(4*2)+(3*7)+(2*8)+(1*8)=179
179 % 10 = 9
So 1219827-88-9 is a valid CAS Registry Number.

1219827-88-9Upstream product

1219827-88-9Downstream Products

1219827-88-9Relevant articles and documents

Hydroformylation reaction of alkylidenecyclopropane derivatives: A new pathway for the formation of acyclic aldehydes containing quaternary stereogenic carbons

Simaan, Samah,Marek, Ilan

, p. 4066 - 4067 (2010)

Figure Presented The rhodium-catalyzed hydroformylation reaction of methylene- and alkylidenecyclopropane derivatives proceeds under mild conditions to lead to the exclusive formation of linear aldehydes and the stereointegrity of the quaternary carbon center remains unaffected in the process. Copyright

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