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102516-38-1

phenyl 3-bromo-1-adamantyl ketone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102516-38-1 Structure

  • Basic information

    1. Product Name: phenyl 3-bromo-1-adamantyl ketone
    2. Synonyms: phenyl 3-bromo-1-adamantyl ketone
    3. CAS NO:102516-38-1
    4. Molecular Formula:
    5. Molecular Weight: 319.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102516-38-1.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: phenyl 3-bromo-1-adamantyl ketone(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl 3-bromo-1-adamantyl ketone(102516-38-1)
    11. EPA Substance Registry System: phenyl 3-bromo-1-adamantyl ketone(102516-38-1)

  • 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: 102516-38-1(Hazardous Substances Data)

102516-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102516-38-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,1 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 102516-38:
(8*1)+(7*0)+(6*2)+(5*5)+(4*1)+(3*6)+(2*3)+(1*8)=81
81 % 10 = 1
So 102516-38-1 is a valid CAS Registry Number.

102516-38-1Relevant articles and documents

BEHAVIOR OF ADAMANTANECARBONYL CHLORIDES IN THE FRIEDEL-CRAFTS REACTION

Yagrushkina, I. N.,Zemtsova, M. N.,Klimochkin, Yu. N.,Moiseev, I. K.

, p. 897 - 900 (2007/10/02)

The reaction of adamantanecarbonyl chlorides with anisole, thiophene, and bithiophene under Friedel-Crafts conditions leads to the formation of ketones.With benzene and toluene the acylation products are only formed with adamantanedicarboxylic acids.The r

SYNTHESIS OF ASYMETRIC DERIVATIVES OF 3,7-DIMETHYLENEBICYCLONONANE

Krasutskii, P. A.,Chesskaya, N. S.,Rodionov, V. N.,Baula, O. P.,Yurchenko, A. G.

, p. 1533 - 1539 (2007/10/02)

The fragmentation of asymmetric dibromo derivatives of adamantane was studied in order to synthesized asymmetric 3,7-dimethylenebicyclononanes.A zinc-copper couple was used as reagent for the fragmentation.During the fragmentation of methyl bromo(3

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