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CAS

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128315-96-8

(3-Aza-bicyclo[3.3.1]non-7-yl)-methanol, also known as 7-hydroxy-3-azabicyclo[3.3.1]nonane, is a chemical compound with a bicyclic structure containing a nitrogen atom. It is used in the synthesis of pharmaceutical compounds and can act as a building block for the development of various drugs. (3-Aza-bicyclo[3.3.1]non-7-yl)-methanol has potential applications in the field of medicinal chemistry, particularly in the creation of drugs targeting the central nervous system. Its unique structure and properties make it a valuable intermediate in organic synthesis and drug discovery processes. Additionally, it has been studied for its potential use in the treatment of neurological disorders and as an antiparkinsonian agent.

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  • 128315-96-8 Structure

  • Basic information

    1. Product Name: (3-Aza-bicyclo[3.3.1]non-7-yl)-methanol
    2. Synonyms: (3-Aza-bicyclo[3.3.1]non-7-yl)-methanol
    3. CAS NO:128315-96-8
    4. Molecular Formula: C9H17NO
    5. Molecular Weight: 155
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 128315-96-8.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-Aza-bicyclo[3.3.1]non-7-yl)-methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-Aza-bicyclo[3.3.1]non-7-yl)-methanol(128315-96-8)
    11. EPA Substance Registry System: (3-Aza-bicyclo[3.3.1]non-7-yl)-methanol(128315-96-8)

  • 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: 128315-96-8(Hazardous Substances Data)

128315-96-8 Usage

Uses

Used in Pharmaceutical Industry:
(3-Aza-bicyclo[3.3.1]non-7-yl)-methanol is used as a building block for the development of various drugs, particularly those targeting the central nervous system. Its unique structure and properties make it a valuable intermediate in organic synthesis and drug discovery processes.
Used in Medicinal Chemistry:
(3-Aza-bicyclo[3.3.1]non-7-yl)-methanol is used in the creation of drugs targeting the central nervous system due to its potential applications in the field of medicinal chemistry.
Used in Neurological Disorders Treatment:
(3-Aza-bicyclo[3.3.1]non-7-yl)-methanol has been studied for its potential use in the treatment of neurological disorders, including its potential as an antiparkinsonian agent.

Check Digit Verification of cas no

The CAS Registry Mumber 128315-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,1 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 128315-96:
(8*1)+(7*2)+(6*8)+(5*3)+(4*1)+(3*5)+(2*9)+(1*6)=128
128 % 10 = 8
So 128315-96-8 is a valid CAS Registry Number.

128315-96-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7α-hydroxymethyl-3-azabicyclo[3.3.1]nonane

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 -
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More Details:128315-96-8 SDS

128315-96-8Downstream Products

128315-96-8Relevant articles and documents

A novel method of synthesis of 1-azaadamantane from 1-boraadamantane

Bubnov, Yu. N.,Gursky, M. E.,Pershin, D. G.

, p. 1 - 8 (2007/10/02)

A novel and convenient method for the synthesis of 1-azaadamantane (I) from the 1-boraadamantane-tetrahydrofuran complex (XIII) is described.This is based on an intramolecular reaction of organic azides with organoboron compounds.Treatment of the boron cage compound XIII with iodine and an excess of sodium azide followed by oxidation (H2O2, OH-) affords 7α-hydroxymethyl-3-azabicyclononane (VII), cyclization of which leads to I in 40percent overall yield.Some new boron cage compounds were also isolated, diazidoborane (XIV) being of particular interest.

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