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CAS

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133566-06-0

1-(7-methoxybicyclo<4.2.0>octa-1,3,5-trien-7-yl)-1-octyn-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133566-06-0 Structure

  • Basic information

    1. Product Name: 1-(7-methoxybicyclo<4.2.0>octa-1,3,5-trien-7-yl)-1-octyn-3-ol
    2. Synonyms:
    3. CAS NO:133566-06-0
    4. Molecular Formula:
    5. Molecular Weight: 258.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133566-06-0.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: 1-(7-methoxybicyclo<4.2.0>octa-1,3,5-trien-7-yl)-1-octyn-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(7-methoxybicyclo<4.2.0>octa-1,3,5-trien-7-yl)-1-octyn-3-ol(133566-06-0)
    11. EPA Substance Registry System: 1-(7-methoxybicyclo<4.2.0>octa-1,3,5-trien-7-yl)-1-octyn-3-ol(133566-06-0)

  • 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: 133566-06-0(Hazardous Substances Data)

133566-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133566-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,6 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133566-06:
(8*1)+(7*3)+(6*3)+(5*5)+(4*6)+(3*6)+(2*0)+(1*6)=120
120 % 10 = 0
So 133566-06-0 is a valid CAS Registry Number.

133566-06-0Upstream product

133566-06-0Downstream Products

133566-06-0Relevant articles and documents

The preparation of α-tetralones from benzocyclobutenones via sequential thermal electrocyclic reactions

Hickman, Derek N.,Wallace, Timothy W.,Wardleworth, J. Michael

, p. 819 - 822 (1991)

1-Alkenylbenzocyclobuten-1-ols, prepared from benzocyclobutenones via the addition of alkenylmagnesium bromides, or the addition of alkynyllithium reagents followed by (E)-selective reduction of the triple bond, undergo successive thermal 4π and 6π electrocyclic reactions leading to substituted 3,4-dihydro-1(2H)-naphthalenones.

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