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5-methyl-2-(4-nitrophenyl)-4,5-dihydro-1,3-oxazole is a chemical compound with the molecular formula C10H10N2O3. It is a derivative of 1,3-oxazole, a heterocyclic compound consisting of a five-membered ring with one oxygen and one nitrogen atom. The molecule features a methyl group (-CH3) at the 5-position, a 4-nitrophenyl group (-C6H4NO2) at the 2-position, and a dihydro (-H2) group at the 4,5-positions. 5-methyl-2-(4-nitrophenyl)-4,5-dihydro-1,3-oxazole is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. Its properties, such as reactivity and stability, make it a valuable building block for the development of new compounds with specific biological activities.

6943-64-2

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6943-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6943-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6943-64:
(6*6)+(5*9)+(4*4)+(3*3)+(2*6)+(1*4)=122
122 % 10 = 2
So 6943-64-2 is a valid CAS Registry Number.

6943-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2-(4-nitrophenyl)-4,5-dihydro-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 2-p-Nitrophenyl-5-methyl-2-oxazolin

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

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More Details:6943-64-2 SDS

6943-64-2Downstream Products

6943-64-2Relevant academic research and scientific papers

Transition metal and base free synthesis of 2-aryl-2-oxazolines from aldehydes and β-amino alcohols catalysed by potassium iodide

Uma Maheswari,Sathish Kumar,Venkateshwar

, p. 39897 - 39900 (2015/02/18)

Synthesis of 2-aryl-2-oxazolines from β-amino alcohols and aldehydes was achieved in good to excellent yield by employing a potassium iodide (KI)-tert-butyl hydroperoxide (TBHP) catalytic system. This protocol is very mild, metal and base free and can be performed under ambient reaction conditions. This oxidative cyclization strategy was further extended for the synthesis of optically active 2-oxazolines, which can act as very useful chiral auxiliaries and as ligands. This journal is

Phosphine-catalyzed heine reaction

Martin, Allen,Casto, Kathleen,Morris, William,Morgan, Jeremy B.

, p. 5444 - 5447 (2011/12/05)

Aziridines are important synthetic intermediates which readily undergo ring-opening reactions. It is demonstrated that electron-rich phosphines are efficient catalysts for the regioselective rearrangement of N-acylaziridines to oxazolines. The reactions o

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