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154419-29-1

6-Allyl-3-methoxymethoxy-cyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154419-29-1 Structure

  • Basic information

    1. Product Name: 6-Allyl-3-methoxymethoxy-cyclohex-2-enone
    2. Synonyms: 6-Allyl-3-methoxymethoxy-cyclohex-2-enone
    3. CAS NO:154419-29-1
    4. Molecular Formula:
    5. Molecular Weight: 196.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154419-29-1.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: 6-Allyl-3-methoxymethoxy-cyclohex-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Allyl-3-methoxymethoxy-cyclohex-2-enone(154419-29-1)
    11. EPA Substance Registry System: 6-Allyl-3-methoxymethoxy-cyclohex-2-enone(154419-29-1)

  • 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: 154419-29-1(Hazardous Substances Data)

154419-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154419-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,4,1 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 154419-29:
(8*1)+(7*5)+(6*4)+(5*4)+(4*1)+(3*9)+(2*2)+(1*9)=131
131 % 10 = 1
So 154419-29-1 is a valid CAS Registry Number.

154419-29-1Downstream Products

154419-29-1Relevant articles and documents

Facile Synthesis of Functionalized Bicyclooctane Systems Using the Selective Fragmentation Reaction

Sagawa, Shoichi,Nagaoka, Hiroto,Yamada, Yasuji

, p. 603 - 604 (1994)

A facile synthesis of two different types of functionalized bicyclooctane systems (kaurane and stachane types) from a tricyclo2,7>octane derivative was performed using the selective fragmentation reaction.

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