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1-BENZYLAZETIDIN-3-ONE, also known as N-benzylazetidin-3-one, is an organic compound characterized by the molecular formula C11H13NO. It features a cyclic amide structure with a benzyl group attached to the nitrogen atom. 1-BENZYLAZETIDIN-3-ONE is recognized for its unique reactivity and structural properties, which render it a valuable intermediate in the synthesis of a wide array of pharmaceuticals and biologically active molecules. Its versatility and potential in medicinal chemistry and drug discovery have garnered significant attention within the scientific community.

156303-83-2

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156303-83-2 Usage

Uses

Used in Pharmaceutical Synthesis:
1-BENZYLAZETIDIN-3-ONE is utilized as a key intermediate for the synthesis of various pharmaceuticals due to its ability to contribute to the formation of diverse heterocyclic compounds and natural products. Its unique structure allows for the creation of complex molecules with potential therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-BENZYLAZETIDIN-3-ONE serves as a building block for the development of new drugs. Its reactivity and structural features facilitate the design and synthesis of compounds with specific biological activities, making it a promising candidate for drug discovery efforts.
Used in the Production of Fine Chemicals:
1-BENZYLAZETIDIN-3-ONE is also used as a component in the manufacturing process of fine chemicals. Its integration into these chemical products enhances their performance and quality, contributing to a range of applications across different industries.
Used in Agrochemicals:
1-BENZYLAZETIDIN-3-ONE finds application in the agrochemical sector as well, where it is employed in the synthesis of various agrochemical products. Its role in this industry is crucial for the development of effective and innovative solutions for agricultural challenges.

Check Digit Verification of cas no

The CAS Registry Mumber 156303-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,0 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156303-83:
(8*1)+(7*5)+(6*6)+(5*3)+(4*0)+(3*3)+(2*8)+(1*3)=122
122 % 10 = 2
So 156303-83-2 is a valid CAS Registry Number.

156303-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BENZYLAZETIDIN-3-ONE

1.2 Other means of identification

Product number -
Other names 1-Benzyl-3-oxo-azetidine

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:156303-83-2 SDS

156303-83-2Downstream Products

156303-83-2Relevant academic research and scientific papers

A new entry towards the synthesis of 1-substituted 3-azetidinones

De Smaele, Dirk,Dejaegher, Yves,Duvey, Guillaume,De Kimpe, Norbert

, p. 2373 - 2375 (2007/10/03)

The synthesis of 1-substituted 3-azetidinones, starting from readily accessible N-(alkylidene)- or N-(arylidene)-2,2,3-tribromopropylamines, is disclosed.

Novel Syntheses of 1,3,3-Trinitroazetidine

Katritzky, Alan R.,Cundy, Darren J.,Chen, Jie

, p. 271 - 276 (2007/10/02)

Alternative methods for the synthesis of 1,3,3-trinitroazetidine (TNAZ) from epichlorohydrin, and benzhydrylamine have been developed.These approaches employ N-sulfonyl-3-(hydroxyimino)azetidines as penultimate intermediates and represent an improvement over previously published methods which require either diazo containing intermediates or involve low yielding procedures.Parallel methods employing N-benzhydryl- and N-benzyl-3-(hydroxyimino)azetidine were also investigated as alternate routes to TNAZ

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