2982-53-8

Basic information

• Product Name: AKOS AU36-M255
• Synonyms: AKOS BBS-00002617;AKOS AU36-M255;(4,5-DIMETHOXY-2-NITRO-PHENYL)-ACETIC ACID METHYL ESTER;2-(4,5-dimethoxy-2-nitrophenyl)acetic acid methyl ester;2-(4,5-dimethoxy-2-nitro-phenyl)acetic acid methyl ester;methyl (4,5-dimethoxy-2-nitrophenyl)acetate;methyl 2-(4,5-dimethoxy-2-nitro-phenyl)ethanoate
• CAS NO: 2982-53-8
• Molecular Formula: C₁₁H₁₃NO₆
• Molecular Weight: 255.22
• Mol File: 2982-53-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 377.4°Cat760mmHg
• Flash Point: 165.1°C
• Appearance: /
• Density: 1.262g/cm³
• Vapor Pressure: 6.76E-06mmHg at 25°C
• Refractive Index: 1.526
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: AKOS AU36-M255(CAS DataBase Reference)
• NIST Chemistry Reference: AKOS AU36-M255(2982-53-8)
• EPA Substance Registry System: AKOS AU36-M255(2982-53-8)

Safety Data

• Hazardous Substances Data: 2982-53-8(Hazardous Substances Data)

Usage

General Description

AKOS AU36-M255 is a chemical compound with the molecular formula C15H10N2O2. It is an off-white solid that is soluble in organic solvents. AKOS AU36-M255 is used as a raw material in the production of various products such as pharmaceuticals, dyes, and agricultural chemicals. It is also used as a reagent in organic synthesis. AKOS AU36-M255 is known for its high purity and quality, making it suitable for a wide range of industrial applications.

InChI:InChI=1/C11H13NO6/c1-16-9-4-7(5-11(13)18-3)8(12(14)15)6-10(9)17-2/h4,6H,5H2,1-3H3

Upstream product

• 67-56-1 methanol 
• 73357-18-3 (4,5-dimethoxy-2-nitrophenyl)acetic acid 
• 73357-23-0 2-(4,5-dimethoxy-2-nitrophenyl)ethan-1-ol 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 
• 15964-79-1 methyl (3,4-dimethoxyphenyl)acetate 

Downstream Products

• 1105512-79-5 methyl 2-(4,5-dimethoxy-2-nitrophenyl)acrylate 
• 73357-27-4 2-nitro-4,5-dimethoxyphenethyl methanesulfonate 
• 177597-14-7 2-nitro-4,5-dimethoxy-N-methylphenethylamine 
• 73357-23-0 2-(4,5-dimethoxy-2-nitrophenyl)ethan-1-ol 
• 57976-61-1 <6-Amino-3.4-dimethoxy-phenyl>-essigsaeure-methylester 

Relevant articles and documents

PIII/PV=O Catalyzed Cascade Synthesis of N-Functionalized Azaheterocycles

An organocatalytic method for the modular synthesis of diverse N-aryl and N-alkyl azaheterocycles (indoles, oxindoles, benzimidazoles, and quinoxalinediones) is reported. The method employs a small-ring organophosphorus-based catalyst (1,2,2,3,4,4-hexamethylphosphetane P-oxide) and a hydrosilane reductant to drive the conversion of ortho-functionalized nitroarenes into azaheterocycles through sequential intermolecular reductive C?N cross coupling with boronic acids, followed by intramolecular cyclization. This method enables the rapid construction of azaheterocycles from readily available building blocks, including a regiospecific approach to N-substituted benzimidazoles and quinoxalinediones.

1,2-disubstituted-6-oxo-3-phenyl-piperidine-3-carboxamides and combinatorial libraries thereof

The invention relates to combinatorial libraries containing two or more novel piperidine-3-carboxamide derivative compounds, methods of preparing the piperidine-3-carboxamide derivative compounds and piperidine-3-carboxamide derivative compounds bound to a resin

Synthesis and biological activity of KCB-328 and its analogues: Novel class III antiarrhythmic agents with little reverse frequency dependence

A series of 3,4-dimethoxyphenethylamine derivatives was prepared, and their prolongation effects on effective refractory period of contractile response (ERPc) and action potential duration (APD) in isolated guinea-pig papillary muscles at 1 Hz and 3 Hz were examined. SAR studies led to the identification of KCB-328 (51) which is a novel class III antiarrhythmic agent with little reverse frequency dependence.