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CAS

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1193090-83-3

7-Benzyl-7-azabicyclo[2.2.1]heptane-1-methanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1193090-83-3 Structure

  • Basic information

    1. Product Name: 7-Benzyl-7-azabicyclo[2.2.1]heptane-1-methanamine
    2. Synonyms: 7-Benzyl-7-azabicyclo[2.2.1]heptane-1-methanamine;7-(phenylmethyl)-7-Azabicyclo[2.2.1]heptane-1-methanamine;(7-Benzyl-7-azabicyclo[2.2.1]heptan-1-yl)methanamine
    3. CAS NO:1193090-83-3
    4. Molecular Formula: C14H20N2
    5. Molecular Weight: 216.322
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1193090-83-3.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: 7-Benzyl-7-azabicyclo[2.2.1]heptane-1-methanamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Benzyl-7-azabicyclo[2.2.1]heptane-1-methanamine(1193090-83-3)
    11. EPA Substance Registry System: 7-Benzyl-7-azabicyclo[2.2.1]heptane-1-methanamine(1193090-83-3)

  • 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: 1193090-83-3(Hazardous Substances Data)

1193090-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1193090-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,3,0,9 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1193090-83:
(9*1)+(8*1)+(7*9)+(6*3)+(5*0)+(4*9)+(3*0)+(2*8)+(1*3)=153
153 % 10 = 3
So 1193090-83-3 is a valid CAS Registry Number.

1193090-83-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (7-benzyl-7-azabicyclo[2.2.1]heptan-4-yl)methanamine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1193090-83-3 SDS

1193090-83-3Relevant articles and documents

A straightforward entry to 7-azabicyclo[2.2.1]heptane-l-carbonitriles in the synthesis of novel epibatidine analogues

Heugebaert, Thomas,Van Hevele, Joke,Couck, Wouter,Bruggeman, Vicky,Van Jeught, Sarah Der,Masschelein, Kurt,Stevens, Christian V.

supporting information; experimental part, p. 1017 - 1020 (2010/04/25)

This paper presents the synthesis of epibatidine analogues by a straightforward one-pot method for the synthesis of 7azabicyclo[2.2.1]heptane-1- carbonitriles, starting from cyclohexanones bearing a leaving group at the 4-position. In situ imine formation

STRAIGHTFORWARD ENTRY TO 7-AZABICYCLO[2.2.1]HEPTANE-1-CARBONITRILES AND SUBSEQUENT SYNTHESIS OF EPIBATIDINE ANALOGUES

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Page/Page column 11-12, (2009/12/02)

The present invention relates to a group of substituted-7-azabicyclo-[2.2.1]heptyl derivatives with biological activity. The present invention also relates to synthetic methods for producing said substituted-7-azabicyclo-[2.2.1]heptyl derivatives. The present invention also relates to certain intermediates for producing such substituted-7-azabicyclo-[2.2.1]heptyl derivatives, as well as a synthetic method for producing such intermediates. The present invention also relates to pharmaceutical compositions comprising such substituted-7-azabicyclo-[2.2.1]heptyl derivatives, as well as their use as medicaments for the treatment of diseases mediated by a Nicotinic Acetylcholine Receptor or a receptor being a member of the Neurotransmitter-gated Ion Channel Superfamily, such as pain, Alzheimer's disease, Parkinson's disease, schizophrenia, epilepsy and nicotine addiction.

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