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5-(chloromethyl)-3-(4-methoxyphenyl)-2-Oxazolidinone is a chemical compound with the molecular formula C10H12ClNO3. It is a derivative of oxazolidinone, a heterocyclic compound consisting of a five-membered ring containing two oxygen atoms and one nitrogen atom. The structure of 5-(chloromethyl)-3-(4-methoxyphenyl)-2-Oxazolidinone features a chloromethyl group at the 5-position, a 4-methoxyphenyl group at the 3-position, and a carbonyl group at the 2-position. 5-(chloromethyl)-3-(4-methoxyphenyl)-2-Oxazolidinone has potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. It is important to handle this chemical with care, as it may have hazardous properties and require proper safety measures during its use and storage.

121082-79-9

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121082-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121082-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,0,8 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121082-79:
(8*1)+(7*2)+(6*1)+(5*0)+(4*8)+(3*2)+(2*7)+(1*9)=89
89 % 10 = 9
So 121082-79-9 is a valid CAS Registry Number.

121082-79-9SDS

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 5-(Chloromethyl)-3-(4-methoxyphenyl)-2-oxazolidinone

1.2 Other means of identification

Product number -
Other names .5-chloromethyl-3-p-methoxyphenyl-oxazolidin-2-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:121082-79-9 SDS

121082-79-9Relevant academic research and scientific papers

A Phosphonium Ylide as a Ligand for [3 + 2] Coupling Reactions of Epoxides with Heterocumulenes under Mild Conditions

Hashimoto, Kousuke,Mori, Yoko,Suga, Hiroyuki,Toda, Yasunori

, p. 10980 - 10987 (2020/09/23)

The potential of carbonyl-stabilized phosphonium ylides as ligands for novel catalysis was explored. We found that the combination of phosphonium ylides and metal halide salts efficiently catalyzed the reaction of epoxides with carbon dioxide under mild c

Tetraarylphosphonium Salt-Catalyzed Synthesis of Oxazolidinones from Isocyanates and Epoxides

Toda, Yasunori,Gomyou, Shuto,Tanaka, Shoya,Komiyama, Yutaka,Kikuchi, Ayaka,Suga, Hiroyuki

supporting information, p. 5786 - 5789 (2017/11/10)

Preparation of a range of oxazolidinones, including enantioenriched N-aryl-substituted oxazolidinones, in which tetraarylphosphonium salts (TAPS) catalyze the [3 + 2] coupling reaction of isocyanates and epoxides effectively, is described. The key finding is a Br?nsted acid/halide ion bifunctional catalyst that can accelerate epoxide ring opening with high regioselectivity. Mechanistic studies disclosed that the ylide generated from TAPS, along with the formation of halohydrins, plays a crucial role in the reaction with isocyanates.

Isocyanurate Formation During Oxazolidinone Synthesis from Epoxides and Isocyanates Catalysed by a Chromium(Salphen) Complex

Wu, Xiao,Mason, Jess,North, Michael

, p. 12937 - 12943 (2017/09/25)

Chromium(salphen) complex 10 is found to be a catalyst for the preparation of oxazolidinones from epoxides and isocyanates. Using the optimal reaction conditions (1.5 mol % of chromium(salphen) complex 10 at 80 °C in toluene for 4 hours), six epoxides wer

Synthesis of Oxazolidinones from Epoxides and Isocyanates Catalysed by Aluminium Heteroscorpionate Complexes

Castro-Osma, José A.,Earlam, Amy,Lara-Sánchez, Agustín,Otero, Antonio,North, Michael

, p. 2100 - 2108 (2016/07/07)

The combination of an aluminium(heteroscorpionate) complex and tetrabutylammonium bromide acts as a highly efficient catalyst system for the synthesis of oxazolidinones from epoxides and isocyanates. Twenty two complexes were tested derived from a range o

VanadiumV(salen) catalysed synthesis of oxazolidinones from epoxides and isocyanates

Beattie, Christopher,North, Michael

, p. 31345 - 31352 (2014/08/05)

The combination of a vanadiumV(salen) complex V +O(salen) EtOSO3- and tetrabutylammonium bromide forms a highly active catalyst system for the reaction between epoxides and isocyanates leading to oxazolidinones.

Bimetallic aluminum(salen) catalyzed synthesis of oxazolidinones from epoxides and isocyanates

Baronsky, Thilo,Beattie, Christopher,Harrington, Ross W.,Irfan, Reyhan,North, Michael,Osende, Javier G.,Young, Carl

, p. 790 - 797 (2013/06/27)

The bimetallic aluminum(salen) complex [Al(salen)]2O is shown to catalyze the synthesis of oxazolidinones from epoxides and isocyanates. The reaction is demonstrated to proceed with overall retention of epoxide stereochemistry, and both aromati

OXAZOLIDINONES

-

, (2008/06/13)

Novel oxazolidinones of the formula I STR1 Z is O or S, R. sup.1 and R 2 are each phenyl or benzyl radicals which are unsubstituted or mono-or disubstituted by alkyl, alkoxy, alkylthio, alkylsulfinyl and/or alkylsulfonyl having each 1-4 C atoms, alkanoylo

Model Studies for the Mechanism of Inactivation of Monoamine Oxidase by 5-(Aminomethyl)-3-aryl-2-oxazolidinones

Gates, Kent S.,Silverman, Richard B.

, p. 8891 - 8895 (2007/10/02)

3-phenyl>-5--2-oxazolidinone (MD 780236) has been reported to be an irreversible inactivator of monoamine oxidase (MAO), but the mechanism of inactivation is not known.A mechanism is now proposed that invol

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