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107909-60-4

N-(α-Adamant-1-ylbenzyl)-α-phenylethylamin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107909-60-4 Structure

  • Basic information

    1. Product Name: N-(α-Adamant-1-ylbenzyl)-α-phenylethylamin
    2. Synonyms:
    3. CAS NO:107909-60-4
    4. Molecular Formula:
    5. Molecular Weight: 345.528
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107909-60-4.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: N-(α-Adamant-1-ylbenzyl)-α-phenylethylamin(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(α-Adamant-1-ylbenzyl)-α-phenylethylamin(107909-60-4)
    11. EPA Substance Registry System: N-(α-Adamant-1-ylbenzyl)-α-phenylethylamin(107909-60-4)

  • 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: 107909-60-4(Hazardous Substances Data)

107909-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107909-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,0 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107909-60:
(8*1)+(7*0)+(6*7)+(5*9)+(4*0)+(3*9)+(2*6)+(1*0)=134
134 % 10 = 4
So 107909-60-4 is a valid CAS Registry Number.

107909-60-4Downstream Products

107909-60-4Relevant articles and documents

Electrochemical Reductive Alkylation of Azomethines with 1-Bromadamantane and 9-Bromo-tetrahydro-exo-dicyclopentadiene

Hess, U.,Lieberenz, C.,Feuerherd, B.

, p. 7 - 20 (2007/10/02)

Electrochemically generated radical anions of Schiffbases 1a-11 react in DMF and in the presence of bridgeheadhalogenides as 1-bromoadamantane and 9-bromo-tetrahydro-exo-dicyclopentadiene to 1--adamantanes and the correspondent 9-tetrahydro-exo-dicyclopentadienes.In the course of SET-mechanism originating bridgehead radicals couple with the azomethine-radicalanions at the position of the highest unpaired electron density, which is predominantly the carbon of the C,N-double bond.Only in cases when this density at the N-atom is relatively high, or steric hindrance impedes C-alkylation, N-hydroalkylated products as N,N-disubstituted 1-aminoadamantanes and 9-amino-tetrahydro-exo-dicyclopentadienes are formed.Product distribution, cyclic-voltammetric results and quantumchemical data are discussed in terms of mechanism.

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