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3-(benzylideneamino)-1,3-oxazolidin-2-one is a chemical compound with the molecular formula C10H10N2O2. It is a derivative of oxazolidinone, a heterocyclic compound containing an oxazolidine ring. This specific compound features a benzylidene group (C6H5-CH=) attached to the nitrogen atom of the oxazolidinone ring, which imparts unique chemical properties and reactivity. It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its ability to form stable derivatives and its potential to act as a chiral auxiliary in asymmetric synthesis. The compound is typically synthesized through the reaction of an appropriate oxazolidinone with a benzaldehyde derivative, followed by dehydration to form the imine linkage. Its structure and properties make it a valuable building block in organic chemistry, particularly in the development of complex molecules with potential applications in medicine and other fields.

4341-14-4

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4341-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4341-14-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4341-14:
(6*4)+(5*3)+(4*4)+(3*1)+(2*1)+(1*4)=64
64 % 10 = 4
So 4341-14-4 is a valid CAS Registry Number.

4341-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(Z)-benzylideneamino]-1,3-oxazolidin-2-one

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

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More Details:4341-14-4 SDS

4341-14-4Relevant academic research and scientific papers

Iron(II)-Catalyzed Radical Addition to Aldimines with Hantzsch Ester as a Two-Hydrogen Atom Donor

Tang, Rui,Shao, Ziyan,Wang, Jiancheng,Liu, Zhongxian,Li, Ya-Min,Shen, Yuehai

, p. 8177 - 8184 (2019)

The first Fe(OTf)2-catalyzed radical addition to aldimines with Hantzsch ester as a two-hydrogen atom donor is reported. The tin-free reaction works well for electron-deficient substrates and provides a potentially useful approach to α-branched

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