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3-benzyl-8-oxa-3-aza-bicyclo[3.2.1]octane is a unique chemical compound characterized by its bicyclic structure, which includes a benzyl group and the presence of oxygen and nitrogen heteroatoms. With a molecular formula of C13H17NO, 3-benzyl-8-oxa-3-aza-bicyclo[3.2.1]octane is derived from a bicyclic framework and may exhibit pharmacological properties due to its structural features, making it a candidate for drug discovery and development. Further research and experimentation are required to explore its specific chemical properties and potential applications.

54745-75-4

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54745-75-4 Usage

Uses

Used in Pharmaceutical Industry:
3-benzyl-8-oxa-3-aza-bicyclo[3.2.1]octane is used as a potential pharmaceutical candidate for drug discovery and development due to its unique structural features and the possibility of possessing pharmacological properties. Its specific applications and therapeutic effects would need to be determined through further research and experimentation.
Used in Chemical Research:
3-benzyl-8-oxa-3-aza-bicyclo[3.2.1]octane is used as a subject of chemical research to investigate its specific chemical properties, potential reactivity, and interactions with other compounds. Understanding these properties can provide insights into its potential applications in various fields, including material science, catalysis, and more.

Check Digit Verification of cas no

The CAS Registry Mumber 54745-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,4 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54745-75:
(7*5)+(6*4)+(5*7)+(4*4)+(3*5)+(2*7)+(1*5)=144
144 % 10 = 4
So 54745-75-4 is a valid CAS Registry Number.

54745-75-4SDS

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 3-Benzyl-8-oxa-3-azabicyclo[3.2.1]octane

1.2 Other means of identification

Product number -
Other names W6898

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:54745-75-4 SDS

54745-75-4Relevant academic research and scientific papers

THIENOPYRIMIDINE AND PYRAZOLOPYRIMIDINE COMPOUNDS AND THEIR USE AS MTOR KINASE AND PI3 KINASE INHIBITORS

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Page/Page column 63, (2009/04/24)

The invention relates to thienopyrimidine and pyrazolopyrimidine compounds of the Formulas (Ia) and (IIa), or a pharmaceutically acceptable salt thereof, wherein the constituent variables are as defined herein compositions comprising the compounds, and methods for making and using the compounds.

8-Oxa-3-azabicyclo(3.2.1)octane analgesic compositions and method of alleviating pain in animals

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, (2008/06/13)

Disclosed are compounds, having the following general formula, which are useful as analgesics in living animals. SPC1 Wherein R is a radical selected from the group consisting of aralkyl, aryl, aminoalkyl, arylalkanoyl, heteroaroyl, alkoxy substituted aroyl, alkenyl (C2 to C4), halogen substituted aralkyl, guanadinoalkyl, halogen substituted aroyl, alkyl substituted aroyl, halogen substituted arylalkanoyl, hexahydrobenzoyl, arylalkenoyl, o- or p-alkyl substituted phenylalkanoyl, alkyl substituted naphthylalkanoyl, alkanoyl (C3 to C20), haloalkyl substituted aroyl, alkoxy substituted aralkyl, heteroaralkyl, anilinocarbonyl, adamantanecarbonyl, arylsulfonyl, carboxyl substituted aroyl, hydroxyl substituted aroyl, alkanoyloxy substituted aroyl, arylglyoxylyl, alicyclic, arylene dicarbonyl-8-oxa-3-azabicyclo(3.2.1)octane, alkylene-8-oxa-3-azabicyclo (3.2.1)octane, alkylene dicarbonyl-8-oxa-3-azabicyclo(3.2.1)octane, and the pharmacologically acceptable acid addition salts thereof.

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