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81465-47-6

3-Iodo-6-isopropyl-2-methyl-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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  • 81465-47-6 Structure

  • Basic information

    1. Product Name: 3-Iodo-6-isopropyl-2-methyl-cyclohex-2-enone
    2. Synonyms:
    3. CAS NO:81465-47-6
    4. Molecular Formula:
    5. Molecular Weight: 278.133
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81465-47-6.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-Iodo-6-isopropyl-2-methyl-cyclohex-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Iodo-6-isopropyl-2-methyl-cyclohex-2-enone(81465-47-6)
    11. EPA Substance Registry System: 3-Iodo-6-isopropyl-2-methyl-cyclohex-2-enone(81465-47-6)

  • 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: 81465-47-6(Hazardous Substances Data)

81465-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81465-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,6 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81465-47:
(7*8)+(6*1)+(5*4)+(4*6)+(3*5)+(2*4)+(1*7)=136
136 % 10 = 6
So 81465-47-6 is a valid CAS Registry Number.

81465-47-6Downstream Products

81465-47-6Relevant articles and documents

Synthesis of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketones

Piers, Edward,Grierson, John R.,Lau, Cheuk Kun,Nagakura, Isao

, p. 210 - 223 (2007/10/02)

A new, efficient method for the preparation of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketones is described.The method involves the reaction of β-diketones or α-hydroxymethylenecycloalkanones with triphenylphosphine dihalides in the presence of trie

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