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CAS

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1415579-77-9

2-(but-3-enyl)-6-hydroxymethylphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415579-77-9 Structure

  • Basic information

    1. Product Name: 2-(but-3-enyl)-6-hydroxymethylphenol
    2. Synonyms:
    3. CAS NO:1415579-77-9
    4. Molecular Formula:
    5. Molecular Weight: 178.231
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415579-77-9.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: 2-(but-3-enyl)-6-hydroxymethylphenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(but-3-enyl)-6-hydroxymethylphenol(1415579-77-9)
    11. EPA Substance Registry System: 2-(but-3-enyl)-6-hydroxymethylphenol(1415579-77-9)

  • 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: 1415579-77-9(Hazardous Substances Data)

1415579-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415579-77-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,5,7 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1415579-77:
(9*1)+(8*4)+(7*1)+(6*5)+(5*5)+(4*7)+(3*9)+(2*7)+(1*7)=179
179 % 10 = 9
So 1415579-77-9 is a valid CAS Registry Number.

1415579-77-9Downstream Products

1415579-77-9Relevant articles and documents

Molecular complexity from aromatics. Cycloaddition of spiroepoxycyclohexa- 2,4-dienones and intramolecular Diels-Alder reaction: A stereoselective entry into tetracyclic core of atisane diterpenoids

Singh, Vishwakarma,Bhalerao, Pravin,Sahu, Bharat Chandra,Mobin, Shaikh M.

, p. 137 - 146 (2013)

A stereoselective approach to tetracyclic core of atisane diterpenoids is described. Oxidative dearomatization, intermolecular cycloaddition of spiroepoxycyclohexa-2,4-dieone with ethyl acrylate, and intramolecular inverse demand π4s+π2s cycloaddition are the key features of our design. Oxidation of appropriately appended o-hydroxymethyl phenols to corresponding 6,6-spiroepoxycyclohexadienones followed by cycloaddition with ethyl acrylate furnished bridged bicyclo[2.2.2]octanes disposed with appropriate functionality. Regioselective manipulation of functional groups led to highly embellished bicyclic systems endowed with appendages containing diene and dienophilic moieties that upon inverse electron demand intramolecular cycloaddition provide the tetracyclic framework of atisanes in stereoselective fashion. A remarkable effect of a remote functional group on intramolecular Diels-Alder reaction has also been described.

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