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syn-11-((allyloxy)carbonyl)-3-(3-hydroxyphenyl)-1,6-methano<10>annulene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 166804-08-6 Structure
  • Basic information

    1. Product Name: syn-11-((allyloxy)carbonyl)-3-(3-hydroxyphenyl)-1,6-methano<10>annulene
    2. Synonyms: syn-11-((allyloxy)carbonyl)-3-(3-hydroxyphenyl)-1,6-methano<10>annulene
    3. CAS NO:166804-08-6
    4. Molecular Formula:
    5. Molecular Weight: 318.372
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 166804-08-6.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: syn-11-((allyloxy)carbonyl)-3-(3-hydroxyphenyl)-1,6-methano<10>annulene(CAS DataBase Reference)
    10. NIST Chemistry Reference: syn-11-((allyloxy)carbonyl)-3-(3-hydroxyphenyl)-1,6-methano<10>annulene(166804-08-6)
    11. EPA Substance Registry System: syn-11-((allyloxy)carbonyl)-3-(3-hydroxyphenyl)-1,6-methano<10>annulene(166804-08-6)
  • 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: 166804-08-6(Hazardous Substances Data)

166804-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166804-08-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,8,0 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 166804-08:
(8*1)+(7*6)+(6*6)+(5*8)+(4*0)+(3*4)+(2*0)+(1*8)=146
146 % 10 = 6
So 166804-08-6 is a valid CAS Registry Number.

166804-08-6Relevant articles and documents

Synthetic studies on the 1,6-methano[10]annulene skeleton: A new route that provides derivatives substituted at the bridge and on the annulene ring

Barrett, David G.,Liang, Gui-Bai,McQuade, D. Tyler,Desper, John M.,Schladetzky, Kurt D.,Gellman, Samuel H.

, p. 10525 - 10532 (2007/10/02)

A new synthetic route to the 1,6-methano[10]annulene skeleton has been developed. The key step in this route is the semi-benzylic Favorskii rearrangement of a [4.4.2]propellane to a [4.4.1]propellane. The methodology discussed here provides access to 1,6-

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