4-Methoxy Pyridine

4-Methoxy Pyridine
4-Methoxy Pyridine
4-Methoxy Pyridine
4-Methoxy Pyridine

4-Methoxy Pyridine

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1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99.9% by HPLC
  • Payment Terms : L/C,T/T,Other

Keywords

Pyridine, 4-methoxy- Iptacopan hydrochloride Iptacopan

Quick Details

  • Appearance:White crystallization
  • Application:Butyldimethylsilyloxyethylcarboxyet
  • PackAge:25kg/drum
  • ProductionCapacity:10|Metric Ton|Day
  • Storage:
  • Transportation:AIR SEA TRAIN

Superiority:

Product Name: 4-Methoxypyridine
Synonyms: gamma-Methoxypyridine;4-METHOXYPYRIDINE;METHYL PYRIDIN-4-YL ETHER;4-METHOXYPYRIDINE, 98+%;4-methoxypridine;Pyridine, 4-methoxy-;4-Methoxypyridine, 99% 5ML;4-Methoxypyridine,99%
CAS: 620-08-6
MF: C6H7NO
MW: 109.13
EINECS: 210-624-7
Product Categories: C6;Heterocyclic Building Blocks;Pyridines, Pyrimidines, Purines and Pteredines;Pyridine series;Pyridine Derivertives;Boronic Acid;blocks;Pyridines;Pyridine
Mol File: 620-08-6.mol
4-Methoxypyridine Structure
 
4-Methoxypyridine Chemical Properties
Melting point  4 °C
Boiling point  108-111 °C/65 mmHg (lit.)
density  1.075 g/mL at 25 °C (lit.)
refractive index  1.518-1.522
Fp  74 °C
storage temp.  Keep in dark place,Sealed in dry,Room Temperature
solubility  DMSO (Slightly), Methanol (Slightly)
form  Liquid
pka 6.58(at 25℃)
Specific Gravity 1.075
color  Clear colorless to slightly yellow
BRN  108211
CAS DataBase Reference 620-08-6(CAS DataBase Reference)
NIST Chemistry Reference Pyridine, 4-methoxy-(620-08-6)
 
Safety Information
Hazard Codes  Xn,Xi
Risk Statements  36/37/38-20/21/22
Safety Statements  37/39-26-36-36/37/39
WGK Germany  3
HS Code  29339900

Details:

4-Methoxypyridine Usage And Synthesis
Chemical Properties clear colorless to slightly yellow liquid
Uses 4-Methoxypyridine, is used as a building block for the synthesis of some biologically active compounds. It is used for the preparation of a new series of benzoylated N-ylides as protein farnesyltransferase inhibitors.
Uses 4-Methoxypyridine was used as a starting reagent for the stereocontrolled synthesis of (±)-pumiliotoxin C and (±)-lasubine II. It was also used in an efficient construction of dihyropyridin-4-ones, which serves as potential ligands for neuronal nicotinic acetycholine receptors.
General Description 4-Methoxypyridine has been prepared from 4-methoxypyridine-N-oxide, via catalytic hydrogenation. Ortho lithiation of 4-methoxypyridine using mesityllithium as the metalating base has been studied.
 
4-Methoxypyridine Preparation Products And Raw materials
Preparation Products 4-N-DECYLPYRIDINE-->3,4-Dimethoxy-2-Methylpyridine-->4-Methoxypiperidine-->3-BROMO-4-METHOXY-PYRIDINE-->2-Bromo-4-methoxypyridine-->4-Methoxypyridine N-oxide-->BENZYL 2-N-PROPYL-4-OXO-3,4-DIHYDROPYRIDINE-1(2H)-CARBOXYLATE-->benzyl 3,4-dihydro-4-oxo-2-phenylpyridine-1(2H)-carboxylate-->PHENYL 4-OXO-2-PHENYL-3,4-DIHYDROPYRIDINE-1(2H)-CARBOXYLATE-->3-Pyridinecarboxaldehyde, 4-methoxy-5-methyl- (9CI)

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