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CAS

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5473-11-0

2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one is a bicyclic ketone chemical compound characterized by a white, crystalline appearance. It possesses a molecular formula of C13H19NO and a molecular weight of 205.29 g/mol. 2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one features a bicyclic structure with a pyrrolidine ring attached to a bicyclo[3.2.1]octane ring, and a ketone functional group at the 8th carbon position. Its unique structure and potential pharmacological properties make it a subject of interest for researchers in the chemical and pharmaceutical industries.

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  • 5473-11-0 Structure

  • Basic information

    1. Product Name: 2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one
    2. Synonyms: 2-Pyrrolidin-1-yl-bicyclo[3.2.1]octan-8-one
    3. CAS NO:5473-11-0
    4. Molecular Formula: C12H19NO
    5. Molecular Weight: 193.2854
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5473-11-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 303.9°C at 760 mmHg
    3. Flash Point: 128.7°C
    4. Appearance: N/A
    5. Density: 1.118g/cm3
    6. Vapor Pressure: 0.000902mmHg at 25°C
    7. Refractive Index: 1.55
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one(5473-11-0)
    12. EPA Substance Registry System: 2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one(5473-11-0)

  • 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: 5473-11-0(Hazardous Substances Data)

5473-11-0 Usage

Uses

Used in Organic Synthesis:
2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one is used as a building block in organic synthesis, contributing to the creation of various complex molecules and compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one is utilized as a key component in the development of new drugs, thanks to its potential therapeutic applications.
Used in Medicinal Chemistry:
2-(pyrrolidin-1-yl)bicyclo[3.2.1]octan-8-one is being investigated for its potential therapeutic applications, with researchers exploring its pharmacological properties to identify possible uses in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 5473-11-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5473-11:
(6*5)+(5*4)+(4*7)+(3*3)+(2*1)+(1*1)=90
90 % 10 = 0
So 5473-11-0 is a valid CAS Registry Number.

5473-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-pyrrolidin-1-ylbicyclo[3.2.1]octan-8-one

1.2 Other means of identification

Product number -
Other names 2-N-pyrrolidylbicyclo<3.2.1>octan-8-one

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:5473-11-0 SDS

5473-11-0Relevant articles and documents

13C-1H Coupling Constants in Carbocations. 5. Trishomocyclopropenium Cations Generated from Bicyclohex-3-yl, Tricyclo2,4>oct-8-yl, and Pentacyclo2,4.03,8.05,7>non-9-yl Precursors

Kelly, David P.,Giansiracusa, Joseph J.,Leslie, D. Ralph,McKern, Ian D.,Sinclair, Georgia C.

, p. 2497 - 2504 (2007/10/02)

One-bond 13C-H coupling constants have been measured for the trismonocyclopropenium cations derived from bicyclohex-3-yl (1), tricyclo2,4>oct-8-yl, (12, 14) and pentacyclo2,4.03,8.05,7>non-9-yl (26, 27) precursors under stable ion conditions and compared with those of the corresponding model ketones. the ΔJ values thus obtained for the bridging carbons (21-32Hz) and the ajacent methylene or methine carbons (18-27 Hz) are large and not consistent with static or equilibrating classical structures for these cations.The data provide additional confirmation of the ??-bridged, nonclassical nature of these

Thermal Rearrangement of 3-Methylenespirododeca-1,4,9-triene and Spirododeca-1,4,9-trien-3-one

Murray, Diane F.,Baum, Mary W.,Jones, Maitland

, p. 1 - 7 (2007/10/02)

Introduction of a double bond into the seven-membered ring of 3-methylenespirododeca-1,4-dien-3-one (1) or spirododeca-1,4-diene (16) alters the thermal behavior of both compounds.Pyrolysis of 3-methylenespirododeca-1,4,9-triene (5) affords the isomeric hydrocarbon cis,cis-2,5-dimethylene-7-vinylbicyclonon-3-ene (11).Pyrolysis of the related ketone spirododeca-1,4,9-trien-3-one (6) gives a mixture of cis,cis-5-methylene-9-vinylbicyclo-3-nonen-2-one (21), cis,cis-5-methylene-7-vinylbicyclo-3-nonen-2-one (22), and trans,trans-2,4,5a,6,8a,8b-hexahydroacenaphthylen-5(1H)-one (23).Mechanistic rationales for these reactions are presented.

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