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1H-Imidazole, 1-(4-methoxyphenyl)-4,5-dimethyl-, 3-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65383-33-7

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65383-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65383-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,8 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65383-33:
(7*6)+(6*5)+(5*3)+(4*8)+(3*3)+(2*3)+(1*3)=137
137 % 10 = 7
So 65383-33-7 is a valid CAS Registry Number.

65383-33-7SDS

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 1-(p-methoxyphenyl)-4,5-dimethyl-1H-imidazole N3-oxide

1.2 Other means of identification

Product number -
Other names 4,5-dimethyl-1-(4-methoxyphenyl)imidazole N3-oxide

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:65383-33-7 SDS

65383-33-7Downstream Products

65383-33-7Relevant academic research and scientific papers

An expeditious synthetic protocol for chlorination of imidazole N-oxide: Synthesis of 2-chloroimidazoles

Hossain, Mossaraf,Pradhan, Kiran,Nanda, Ashis Kumar

supporting information, p. 3772 - 3776 (2017/09/09)

An expeditious, one-pot and room temperature protocol is reported for the synthesis of 2-chloroimidazoles from imidazole N-oxide. Simple mixing of the imidazole N-oxide, derived easily from diacetyl monoxime via three-component reaction, with oxalyl chlor

Synthesis of 2-unsubstituted 1-arylimidazoles

Mityanov,Perevalov,Tkach

, p. 1793 - 1800 (2013/07/26)

A method has been developed for the synthesis of 1-arylimidazoles lacking a substituent at position 2, featuring the preparation of 1-arylimidazole N-oxides stabilized as boron trifluoride derivatives, with subsequent reduction to the desired imidazoles. This method permits broad variation of the substituents in the aryl part of these molecules.

Novel antiprotozoal products: imidazole and benzimidazole N-oxide derivatives and related compounds.

Aguirre, Gabriela,Boiani, Mariana,Cerecetto, Hugo,Gerpe, Alejandra,Gonzalez, Mercedes,Sainz, Yolanda Fernandez,Denicola, Ana,De Ocariz, Carmen Ochoa,Nogal, Juan Jose,Montero, David,Escario, Jose Antonio

, p. 259 - 270 (2007/10/03)

The syntheses and biological evaluation of the first anti-protozoa imidazole N-oxide and benzimidazole N-oxide and their derivatives are reported. They were tested in vitro against two different protozoa, Trypanosoma cruzi and Trichomonas vaginalis. Deriv

New synthetic approach for the preparation of imidazole N3-oxide

Cerecetto, Hugo,Gerpe, Alejandra,Gonzalez, Mercedes,Fernandez Sainz, Yolanda,Piro, Oscar E.,Castellano, Eduardo E.

, p. 2678 - 2684 (2007/10/03)

A new synthetic procedure of 1-alkyl(aryl)-1H-4-methylimidazole N 3-oxide derivatives by cyclocondensation of α-amineoximes and orthoesters was studied. Low yields in the cyclization process were the result of predominant Z-stereoisomer around the oxime moiety of α-amineoxime reactants. Different attempts to improve these yields were assayed, mild conditions being those that produce the best results. Also, the special acidity of hydrogen-2 in the imidazole N3-oxide system was studied in solution by NMR spectroscopy. This property provides a convenient intermediate to access 2-substituted analogues.

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