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CAS

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778581-74-1

3-BENZYL-8,8-DIMETHOXY-3-AZABICYCLO[3.2.1]OCTANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 778581-74-1 Structure

  • Basic information

    1. Product Name: 3-BENZYL-8,8-DIMETHOXY-3-AZABICYCLO[3.2.1]OCTANE
    2. Synonyms: 3-BENZYL-8,8-DIMETHOXY-3-AZABICYCLO[3.2.1]OCTANE
    3. CAS NO:778581-74-1
    4. Molecular Formula: C16H23NO2
    5. Molecular Weight: 261.35932
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 778581-74-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-BENZYL-8,8-DIMETHOXY-3-AZABICYCLO[3.2.1]OCTANE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-BENZYL-8,8-DIMETHOXY-3-AZABICYCLO[3.2.1]OCTANE(778581-74-1)
    11. EPA Substance Registry System: 3-BENZYL-8,8-DIMETHOXY-3-AZABICYCLO[3.2.1]OCTANE(778581-74-1)

  • 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: 778581-74-1(Hazardous Substances Data)

778581-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 778581-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,8,5,8 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 778581-74:
(8*7)+(7*7)+(6*8)+(5*5)+(4*8)+(3*1)+(2*7)+(1*4)=231
231 % 10 = 1
So 778581-74-1 is a valid CAS Registry Number.

778581-74-1Relevant articles and documents

THERAPEUTICALLY ACTIVE BICYCLIC-SULPHONAMIDES AND PHARMACEUTICAL COMPOSITIONS

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Paragraph 0096, (2019/05/18)

Pharmaceutical compounds have a bicyclic-sulphonamide structure and pharmaceutical compositions including the compounds may be used in therapy as brain-cell-death protectants and may be used, for example, in the treatment of chronic neurodegenerative diseases. The compounds are active as inhibitors of N-acylethanolamine-hydrolysing acid amidase (NAAA) and may be used for the therapeutic treatment and prevention of pain and inflammatory disorders and other disorders which benefit from the modulation of fatty acid ethanolamides, particularly palmitoylethanolamide (PEA).

Aza bicycloderivative, preparation and application thereof

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, (2019/04/27)

The invention discloses an aza bicycloderivative, preparation and an application thereof. The aza bicycloderivative has a structure shown in formula I, wherein the definition of all substituted groupsis described in specification and claims. The compound

An approach to azabicyclo[ n.3.1]alkanes by double mannich reaction

Mityuk, Andrey P.,Denisenko, Aleksandr V.,Dacenko, Oleksandr P.,Grygorenko, Oleksandr O.,Mykhailiuk, Pavel K.,Volochnyuk, Dmitriy M.,Shishkin, Oleg V.,Tolmachev, Andrey A.

experimental part, p. 493 - 497 (2010/04/26)

Chlorotrimethylsilane-promoted double Mannich annulation of ketones using N,N-bis(methoxymethyl)benzylamine has been explored. It has been shown that the structure of the substrate drastically influenced the outcome of the reaction. The method allows azabicyclo[n.3.1]alkane derivatives (n=2-5) to be obtained in good yields. Georg Thieme Verlag Stuttgart New York.

METHOD FOR PRODUCING PIPERIDIN-4-ONE-DERIVATIVE

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Page/Page column 13-14, (2009/06/27)

Provided is a method for producing a piperidin-4-one derivative useful as an intermediate for agricultural chemicals or pharmaceutical products. A piperidin-4-one derivative represented by formula (III-a) or formula (III-b) is produced by reacting a cycli

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