127446-35-9

Basic information

• Product Name: N-(4-FORMYL-PYRIDIN-3-YL)-2,2-DIMETHYL-PROPIONAMIDE
• Synonyms: N-(4-FORMYL-PYRIDIN-3-YL)-2,2-DIMETHYL-PROPIONAMIDE;N-(4-FORMYL-PYRIDIN-;N-(4-ForMylpyridin-3-yl)pivalaMide;N-(4-formylpyridin-3-yl)-2,2-dimethylpropanamide
• CAS NO: 127446-35-9
• Molecular Formula: C11H14N2O2
• Molecular Weight: 206.24
• Product Categories: pharmacetical
• Mol File: 127446-35-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 76-77°C
• Boiling Point: 394.3ºC at 760 mmHg
• Flash Point: 192.3 ºC
• Appearance: /
• Density: 1.165 g/cm³
• Vapor Pressure: 2E-06mmHg at 25°C
• Refractive Index: 1.584
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 13.68±0.70(Predicted)
• CAS DataBase Reference: N-(4-FORMYL-PYRIDIN-3-YL)-2,2-DIMETHYL-PROPIONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-FORMYL-PYRIDIN-3-YL)-2,2-DIMETHYL-PROPIONAMIDE(127446-35-9)
• EPA Substance Registry System: N-(4-FORMYL-PYRIDIN-3-YL)-2,2-DIMETHYL-PROPIONAMIDE(127446-35-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36-43
• Safety Statements: 26-36/37
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 127446-35-9(Hazardous Substances Data)

Usage

General Description

N-(4-Formyl-pyridin-3-yl)-2,2-dimethyl-propionamide is a chemical compound with the molecular formula C13H15N3O2. It is a derivative of pyridine and is used in research as a building block for the synthesis of various pharmaceutical and agrochemical compounds. The compound is known for its potential bioactivity and is used in the development of new drugs and pesticides. It is typically synthesized through organic chemical reactions and is available for purchase from chemical suppliers for use in laboratory and industrial applications.

InChI:InChI=1/C11H14N2O2/c1-11(2,3)10(15)13-9-6-12-5-4-8(9)7-14/h4-7H,1-3H3,(H,13,15)

Upstream product

• 70298-88-3 N-(pyridin-3-yl)pivalamide 
• 68-12-2 N,N-dimethyl-formamide 

Relevant articles and documents

Modified aminoacids, pharmaceuticals containing these compounds and method for their production

The present invention relates to modified amino acids of general formula wherein A, Z, X, n, m, R, R2, R3, R4and R11are defined as in claims 1 to 5, their tautomers, their diastereomers, their enantiomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, pharmaceutical compositions containing these compounds, the use thereof and processes for preparing them as well as their use for the production and purification of antibodies and as labelled compounds in RIA- and ELISA assays and as diagnostic or analytical aids in neurotransmitter research.

A General Approach to the Synthesis of 1,6-, 1,7-, and 1,8-Naphthyridines

A new three-step procedure for pyridine annulation is described and illustrated with efficient syntheses of various 1,6-, 1,7-, and 1,8-naphthyridin-2-ones as well as 6-chloroquinolin-2-one.The regiospecific ortho metalation and subsequent formylation of