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CAS

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63623-82-5

2-(1-Adamantyl)-2-hydroxyacetophenon is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63623-82-5 Structure

  • Basic information

    1. Product Name: 2-(1-Adamantyl)-2-hydroxyacetophenon
    2. Synonyms:
    3. CAS NO:63623-82-5
    4. Molecular Formula:
    5. Molecular Weight: 270.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63623-82-5.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: 2-(1-Adamantyl)-2-hydroxyacetophenon(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-Adamantyl)-2-hydroxyacetophenon(63623-82-5)
    11. EPA Substance Registry System: 2-(1-Adamantyl)-2-hydroxyacetophenon(63623-82-5)

  • 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: 63623-82-5(Hazardous Substances Data)

63623-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63623-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,6,2 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63623-82:
(7*6)+(6*3)+(5*6)+(4*2)+(3*3)+(2*8)+(1*2)=125
125 % 10 = 5
So 63623-82-5 is a valid CAS Registry Number.

63623-82-5Downstream Products

63623-82-5Relevant articles and documents

Modification of Photochemical Reactivity by Cyclodextrin Complexation: Product Selectivity in Photo-Fries Rearrangement

Syamala, M. S.,Rao, B. Nageswer,Ramamurthy, V.

, p. 7234 - 7242 (2007/10/02)

Cyclodextrin encapsulation, both in the solid state and in aqueous solution brings about a remarkable regulation of the photo-Fries rearrangement of phenyl esters and anilides.In comparison to the non-selective mixture of ortho and para-rearranged isomers along with the deacylated product obtained in organic solvents, the solid β-cyclodextrin complexes of unsubstituted esters and anilides show a remarkable 'ortho-selectivity'.An impressive 'regio-selectivity' among the two ortho-rearranged isomers is observed for meta-substituted esters and anilides upon irradiation as β-cyclodextrin complexes.Specific orientations of the unsubstituted and meta-substituted esters and anilides in the β-cyclodextrin cavity are suggested to be responsible for the observed selectivity.

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