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CAS

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86853-96-5

13H-indeno[1,2-l]phenanthren-13-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86853-96-5 Structure

  • Basic information

    1. Product Name: 13H-indeno[1,2-l]phenanthren-13-one
    2. Synonyms:
    3. CAS NO:86853-96-5
    4. Molecular Formula:
    5. Molecular Weight: 280.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86853-96-5.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: 13H-indeno[1,2-l]phenanthren-13-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 13H-indeno[1,2-l]phenanthren-13-one(86853-96-5)
    11. EPA Substance Registry System: 13H-indeno[1,2-l]phenanthren-13-one(86853-96-5)

  • 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: 86853-96-5(Hazardous Substances Data)

86853-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86853-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,5 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86853-96:
(7*8)+(6*6)+(5*8)+(4*5)+(3*3)+(2*9)+(1*6)=185
185 % 10 = 5
So 86853-96-5 is a valid CAS Registry Number.

86853-96-5Downstream Products

86853-96-5Relevant articles and documents

Direct intramolecular arylation of aldehydes promoted by reaction with IPy2BF4/HBF4: Synthesis of benzocyclic ketones

Barluenga, Jose,Trincado, Monica,Rubio, Eduardo,Gonzalez, Jose M.

, p. 3140 - 3143 (2006)

(Chemical Equation Presented) Iodine helps: Aldehydes acylate arenes upon treatment at low temperature with IPy2BF4 and HBF 4. This reaction is exploited in a novel intramolecular approach to the preparation of benzocyclic ketones (see scheme). A plausible mechanistic rational is also given.

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