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1201810-92-5

C18H22O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1201810-92-5 Structure

  • Basic information

    1. Product Name: C18H22O2
    2. Synonyms: C18H22O2
    3. CAS NO:1201810-92-5
    4. Molecular Formula:
    5. Molecular Weight: 270.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1201810-92-5.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: C18H22O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H22O2(1201810-92-5)
    11. EPA Substance Registry System: C18H22O2(1201810-92-5)

  • 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: 1201810-92-5(Hazardous Substances Data)

1201810-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201810-92-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,8,1 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1201810-92:
(9*1)+(8*2)+(7*0)+(6*1)+(5*8)+(4*1)+(3*0)+(2*9)+(1*2)=95
95 % 10 = 5
So 1201810-92-5 is a valid CAS Registry Number.

1201810-92-5Downstream Products

1201810-92-5Relevant articles and documents

Catalytic enantioselective formation of chiral-bridged dienes which are themselves ligands for enantioselective catalysis

Brown, M. Kevin,Corey

supporting information; experimental part, p. 172 - 175 (2010/03/30)

"Chemical Equation Presented" This paper reports a method for highly enantioselective Diels-Alder reaction with an acetylene equivalent to produce chiral-bridged dienes. These dienes, by coordination to Rh(I), can serve as catalysts for the enantioselective addition of vinyl or aryl groups to (aryl-unsaturated ketones

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