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273207-58-2

Exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol is a complex chemical compound characterized by its bicyclic ring system, featuring a Boc-protected amine group and a hydroxyl group on the third carbon. The "exo" designation signifies that the bulky substituents are positioned on the same side of the ring as the bridge, which can affect the compound's reactivity and interactions with other molecules. This unique structure makes it a valuable building block in medicinal chemistry and organic synthesis for the development of pharmaceuticals and bioactive compounds.

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  • 273207-58-2 Structure

  • Basic information

    1. Product Name: exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol
    2. Synonyms: exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol;(3-exo)-tert-Butyl 3-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate
    3. CAS NO:273207-58-2
    4. Molecular Formula: C13H23NO3
    5. Molecular Weight: 241.32662
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 273207-58-2.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: exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol(273207-58-2)
    11. EPA Substance Registry System: exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol(273207-58-2)

  • 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: 273207-58-2(Hazardous Substances Data)

273207-58-2 Usage

Uses

Used in Medicinal Chemistry:
Exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol is used as a building block for the synthesis of various pharmaceuticals and bioactive compounds. Its exo-configuration and Boc protection influence its reactivity, allowing for the creation of new molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol serves as a versatile intermediate for the preparation of complex organic molecules. Its unique structure and functional groups enable the synthesis of a wide range of compounds with diverse properties and applications.
Used in Drug Development:
Exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol is utilized in drug development as a key component in the design and synthesis of novel therapeutic agents. Its ability to form stable intermediates and its compatibility with various chemical reactions make it an attractive candidate for the creation of new drugs with improved efficacy and selectivity.
Used in Chemical Research:
In the realm of chemical research, exo-8-Boc-8-azabicyclo[3.2.1]octane-3-Methanol is employed as a model compound to study the effects of ring strain, stereochemistry, and functional group interactions on molecular properties and reactivity. This research can provide valuable insights into the design of new synthetic routes and the development of innovative chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 273207-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,3,2,0 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 273207-58:
(8*2)+(7*7)+(6*3)+(5*2)+(4*0)+(3*7)+(2*5)+(1*8)=132
132 % 10 = 2
So 273207-58-2 is a valid CAS Registry Number.

273207-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (exo)-3-hydroxymethyl-8-azabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names tert-butyl exo-3-hydroxymethyl-8-azabicyclo[3.2.1]octane-8-carboxylate

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:273207-58-2 SDS

273207-58-2Upstream product

273207-58-2Relevant articles and documents

Functional Group Interconversion of Alkylidenemalononitriles to Primary Alcohols by a Cooperative Redox Operation

Emmetiere, Fabien,Grenning, Alexander J.

, p. 3077 - 3085 (2020/08/10)

Functional group interconversions are essential chemical processes enabling synthesis. In this report, we describe a strategy to convert alkylidenemalononitriles into primary alcohols in one step. The reaction relies on a choreographed redox process invol

1H-IMIDAZOPYRIDINE DERIVATIVES

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, (2008/06/13)

A 1H-imidazopyridine derivative represented by the following general formula (I) or a salt thereof having an inhibitory action against production of a cytokine: wherein R1 represents hydrogen atom, an alkyl group, a cycloalkyl group, or an aryl

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