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N-(5-nitrofurfurylidene)-p-anisidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74675-72-2

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74675-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74675-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,7 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74675-72:
(7*7)+(6*4)+(5*6)+(4*7)+(3*5)+(2*7)+(1*2)=162
162 % 10 = 2
So 74675-72-2 is a valid CAS Registry Number.

74675-72-2Downstream Products

74675-72-2Relevant academic research and scientific papers

Solvatochromism of dyes inspired in Effenberger's probe

Domínguez, Moisés,Machado, Vanderlei G.,Rezende, Marcos C.,de Melo, Carlos E. A.

, (2021)

Solvatochromic dyes have been utilized in recent decades as probes to measure the polarity of the medium. An interesting example is the Effenberger's dye (ED), which exhibits a very pronounced positive solvatochromism, being considered a dye that probes p

Antibacterial action of (5-nitrofurfuryl)-derived aminophosphonates and their parent imines

Lewkowski, Jaros?aw,Morawska, Marta,Kowalczyk, Aleksandra

, p. 365 - 374 (2019/02/14)

Abstract: Ten aminophosphonates bearing 2-nitrofuran moiety and two N-aryl 5-nitro-furfuralaldimines, namely, N-(2-nitrofurfurylidene)-p-toluidine and N-(2-nitrofurfurylidene)-p-anisidine, were tested in aspect of their antibacterial action. O,O′-diphenyl

Mixed carboxylic-sulfonic anhydride in reaction with imines: A straightforward route to water-soluble β-lactams via a Staudinger-type reaction

Bakulina, Olga,Dar'In, Dmitry,Krasavin, Mikhail

, p. 3989 - 3998 (2018/06/08)

The first example of employing a mixed carboxylic-sulfonic anhydride in reaction with imines is reported. Unlike its well-studied isostere homophthalic anhydride, benzo[c][1,2]oxathiin-3(4H)-one 1,1-dioxide gave no product of a formal [4 + 2] cycloaddition and only followed an alternative reaction pathway toward β-lactams, presumably, via a formal [2 + 2] cycloaddition (a Staudinger-type reaction). Optimized reaction conditions involve the use of triethylamine as a base promoter, which also allows isolating the product β-lactam benzene sulfonic acids as respective triethylammonium salts by conventional column chromatography. The reaction shows some preference to trans-isomer formation; pure diastereomers can be isolated in some cases.

Enantioselective synthesis of 1,2,5,6-tetrahydropyridines (THPs): Via proline-catalyzed direct Mannich-cyclization/domino oxidation-reduction sequence: Application for medicinally important N-heterocycles

Ramaraju, Panduga,Mir, Nisar A.,Singh, Deepika,Kumar, Indresh

, p. 60422 - 60432 (2016/07/11)

An enantioselective multi-component synthesis of 1,2,5,6-tetrahydropyridines (THPs) has been developed through a one-pot domino-process. This transformation proceeds through proline-catalyzed direct Mannich reaction-cyclization of glutaraldehyde with in s

SOME DATA ON THE CHEMISTRY OF 5-NITRO-2-FURALDEHYDE, V. ANILINE DERIVATIVES

Csaszar, Jozsef

, p. 245 - 258 (2007/10/02)

UV, IR and 1H-NMR spectra of Schiff bases of 5-nitro-2-furaldehyde with mono- and disubstituted anilines have been investigated.The spectra measured in methanol, in acidic and basic media and in concentrated sulfuric acid are discussed in conne

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