42564-41-0 Usage
General Description
4-Methylamino-3-Nitro-Benzaldehyde (MNB) is an organic compound that exists as a yellow crystalline powder and belongs to the class of chemical entities known as nitrobenzenes. These are compounds containing a nitro group attached to a benzene ring. MNB features a nitro group (NO2) and a methylamino group (NH2CH3) attached to the benzene ring, alongside an aldehyde group (-CHO). MNB is primarily used in various research and development settings, specifically in the synthesis of other complex compounds and as a reagent in chemical reactions. It is typically used in laboratory conditions due to its potentially hazardous nature when not handled properly. Its precise physical, biological, and toxicological properties are under research.
Check Digit Verification of cas no
The CAS Registry Mumber 42564-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,6 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 42564-41:
(7*4)+(6*2)+(5*5)+(4*6)+(3*4)+(2*4)+(1*1)=110
110 % 10 = 0
So 42564-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O3/c1-9-7-3-2-6(5-11)4-8(7)10(12)13/h2-5,9H,1H3
42564-41-0Relevant articles and documents
Metalloporphyrin and heteropoly acid catalyzed oxidation of C=NOH bonds in an ionic liquid: Biomimetic models of nitric oxide synthase
Jain, Nidhi,Kumar, Anil,Chauhan, Shive M.S.
, p. 2599 - 2602 (2007/10/03)
Water soluble iron(III) porphyrins and phosphotungstic acid in an ionic liquid are effective catalysts for the H2O2 mediated oxidation of the CNOH bond in N-hydroxyarginine and other oximes. The carbonyl compounds generated as the oxidation products can be easily isolated from the reaction media. These systems serve as biomimetic models of nitric oxide synthase (NOS) and the catalyst immobilized in an ionic liquid can be easily recycled and reused.
Artificial Redox Enzymes. 1. Synthetic Strategies
Rong, Ding,Ye, Hongping,Boehlow, Todd R.,D'Souza, Valerian T.
, p. 163 - 167 (2007/10/02)
Organic models of flavoenzymes consist of a binding site covalently attached to a flavin derivative acting as the catalytic site.The earlier reported synthesis of such a model using α-cyclodextrin as the binding site proved to be difficult to reproduce wi
