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CAS

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76016-04-1

(Z)-3-Methyl-5-(2,3,6-trimethyl-phenyl)-pent-2-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76016-04-1 Structure

  • Basic information

    1. Product Name: (Z)-3-Methyl-5-(2,3,6-trimethyl-phenyl)-pent-2-en-1-ol
    2. Synonyms:
    3. CAS NO:76016-04-1
    4. Molecular Formula:
    5. Molecular Weight: 218.339
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76016-04-1.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: (Z)-3-Methyl-5-(2,3,6-trimethyl-phenyl)-pent-2-en-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-3-Methyl-5-(2,3,6-trimethyl-phenyl)-pent-2-en-1-ol(76016-04-1)
    11. EPA Substance Registry System: (Z)-3-Methyl-5-(2,3,6-trimethyl-phenyl)-pent-2-en-1-ol(76016-04-1)

  • 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: 76016-04-1(Hazardous Substances Data)

76016-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76016-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,1 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76016-04:
(7*7)+(6*6)+(5*0)+(4*1)+(3*6)+(2*0)+(1*4)=111
111 % 10 = 1
So 76016-04-1 is a valid CAS Registry Number.

76016-04-1Downstream Products

76016-04-1Relevant articles and documents

Laurencia sesquiterpene biogenetic-type interconversions

Gonzalez,Darias,Martin,Martin,Norte,Perez,Perales,Fayos

, p. 1151 - 1154 (1980)

Several aromatic sesquiterpenes from Laurencia algae were prepared from chamigrene skeleton precursors. Chemical evidence was adduced to support a biogenetic-type scheme for the synthesis of perforenol and perforene. By means of x ray analysis the structure and absolute configuration of one of the intermediates was established.

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