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CAS

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1213781-29-3

C15H16O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1213781-29-3 Structure

  • Basic information

    1. Product Name: C15H16O2
    2. Synonyms:
    3. CAS NO:1213781-29-3
    4. Molecular Formula:
    5. Molecular Weight: 228.291
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1213781-29-3.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: C15H16O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H16O2(1213781-29-3)
    11. EPA Substance Registry System: C15H16O2(1213781-29-3)

  • 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: 1213781-29-3(Hazardous Substances Data)

1213781-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1213781-29-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,3,7,8 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1213781-29:
(9*1)+(8*2)+(7*1)+(6*3)+(5*7)+(4*8)+(3*1)+(2*2)+(1*9)=133
133 % 10 = 3
So 1213781-29-3 is a valid CAS Registry Number.

1213781-29-3Upstream product

1213781-29-3Downstream Products

1213781-29-3Relevant articles and documents

A new synthesis of 8-oxabicyclo[3.2.1]octan-2-one and its use for the preparation of cycloheptane annulated furans

Hopf, Henning,Abhilash

experimental part, p. 3349 - 3351 (2010/03/04)

Two novel syntheses of 8-oxabicyclo[3.2.1]octan-2-one are described, making this key intermediate readily available in preparative amounts. On chain elongation with various oxophosphonates this compound is converted to α,β-unsaturated ketones, which, on t

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