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3-(Benzyl-methyl-amino)-indan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 52459-01-5 Structure
  • Basic information

    1. Product Name: 3-(Benzyl-methyl-amino)-indan-1-one
    2. Synonyms: 3-(Benzyl-methyl-amino)-indan-1-one
    3. CAS NO:52459-01-5
    4. Molecular Formula:
    5. Molecular Weight: 251.328
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 52459-01-5.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: 3-(Benzyl-methyl-amino)-indan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(Benzyl-methyl-amino)-indan-1-one(52459-01-5)
    11. EPA Substance Registry System: 3-(Benzyl-methyl-amino)-indan-1-one(52459-01-5)
  • 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: 52459-01-5(Hazardous Substances Data)

52459-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52459-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,5 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52459-01:
(7*5)+(6*2)+(5*4)+(4*5)+(3*9)+(2*0)+(1*1)=115
115 % 10 = 5
So 52459-01-5 is a valid CAS Registry Number.

52459-01-5Relevant articles and documents

SYNTHESIS OF DERIVATIVES STRUCTURALLY RELATED TO GLAZIOVINE

Bellamy, F. D.,Chazan, J. B.,Ou, K.

, p. 2803 - 2806 (2007/10/02)

Three compounds, 2a, 2b, and 2c have been synthesized by an analogy with glaziovine 1 which has been claimed to have anxiolytic properties similar to diazepam.The intermediates indanones 5 have been obtained according to conventional (for 5a) or less conventional procedure (5b) and then converted to the corresponding indanones 11.Michael addition of methylbenzylamine followed by a one-carbon homologation of the ketone gave an aldehyde suitable for Robinson annulation leading to the spiro compounds 2.DDQ oxidation gave 3.No anxiolytic activity was found from the pharmacological data.

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