ChemicalBook > CAS DataBase List > 4-Methoxy-3-pyridinecarboxaldehyde

4-Methoxy-3-pyridinecarboxaldehyde

Product Name
4-Methoxy-3-pyridinecarboxaldehyde
CAS No.
82257-15-6
Chemical Name
4-Methoxy-3-pyridinecarboxaldehyde
Synonyms
4-Methoxynicotinaldehyde;4-MethoxynicotinaL;3-FORMYL-4-METHOXYPYRIDINE;4-METHOXY-PYRIDINE-3-CARBALDEHYE;4-Methoxypyridine-3-carbaldehyde;4-Methoxy-3-carboxaldehydepyridine;4-METHOXYPYRIDINE-3-CARBOXALDEHYDE;4-METHOXY-3-PYRIDINE CARBOXALDEHYDE;3-Pyridinecarboxaldehyde, 4-Methoxy-;3-Pyridinecarboxaldehyde, 4-methoxy- (9CI)
CBNumber
CB7488696
Molecular Formula
C7H7NO2
Formula Weight
137.14
MOL File
82257-15-6.mol
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4-Methoxy-3-pyridinecarboxaldehyde Property

Melting point:
63-67°C
Boiling point:
262.9±20.0 °C(Predicted)
Density 
1.159±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
4.75±0.18(Predicted)
Appearance
White to yellow Solid
CAS DataBase Reference
82257-15-6(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
HazardClass 
IRRITANT
HS Code 
2933399990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H226Flammable liquid and vapour

H320Causes eye irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P241Use explosion-proof electrical/ventilating/lighting/…/equipment.

P242Use only non-sparking tools.

P243Take precautionary measures against static discharge.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P337+P313IF eye irritation persists: Get medical advice/attention.

P370+P378In case of fire: Use … for extinction.

P403+P235Store in a well-ventilated place. Keep cool.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

TRC
Product number
M267155
Product name
4-Methoxypyridine-3-carboxaldehyde
Packaging
100mg
Price
$120
Updated
2021/12/16
Matrix Scientific
Product number
053825
Product name
4-Methoxynicotinaldehyde
Packaging
500mg
Price
$150
Updated
2021/12/16
Matrix Scientific
Product number
053825
Product name
4-Methoxynicotinaldehyde
Packaging
2.500g
Price
$375
Updated
2021/12/16
Matrix Scientific
Product number
053825
Product name
4-Methoxynicotinaldehyde
Packaging
1g
Price
$250
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
59910
Product name
4-Methoxypyridine-3-carboxaldehyde
Packaging
100mg
Price
$610
Updated
2021/12/16
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4-Methoxy-3-pyridinecarboxaldehyde Chemical Properties,Usage,Production

Chemical Properties

light yellow solid

Uses

4-Methoxypyridine-3-carboxaldehyde, is an intermediate for the synthesis of 4-Hydroxy-3-pyridinecarboxylic Acid (H952780). It can also be used for the preparation of 7,8-dimethylquinolines derivatives as potential antimicrobial and antifungal agents.

Synthesis

620-08-6

68-12-2

82257-15-6

Example 2 Preparation of 4-methoxypyridine-3-carbaldehyde To a stirred solution of tetrahydrofuran (380 mL) was added tert-butyllithium (90.6 mL, 154 mmol; 1.7 M in pentane) via cannula under nitrogen protection. The reaction mixture was cooled to -78°C, followed by dropwise addition of 2-bromotoluene (11.3 mL, 74.1 mmol). The reaction mixture was stirred at -78°C for 1 hour. Then, 4-methoxypyridine (5.79 mL, 57 mmol) was added dropwise to the reaction mixture at -78°C and the resulting mixture was stirred at -23°C for 3 hours. The reaction mixture was again cooled to -78°C, N,N-dimethylformamide (6.62 mL, 85.5 mmol) was added and stirring was continued at -78°C for 1 hour. The reaction mixture was slowly quenched with saturated aqueous sodium chloride solution (100 mL) at -78°C, followed by slow warming to room temperature. Ether (200 mL) was added to the reaction mixture and the organic and aqueous layers were separated. The aqueous layer was extracted with ether (2 x 150 mL) and the combined organic layers were dried with anhydrous potassium carbonate (20 g). The potassium carbonate was removed by filtration, the filter cake was washed with ether (100 mL), and the solvent was removed by concentration under reduced pressure. The resulting crude product, 4-methoxy-3-pyridinecarboxaldehyde, was purified by silica gel column chromatography (eluent ratio 5:95 ethanol:ethyl acetate) to afford 4.79 g of the target product as a yellow solid (61% yield; purity >98% as determined by 1H NMR).

References

[1] Tetrahedron Letters, 2006, vol. 47, # 1, p. 39 - 41
[2] Tetrahedron Letters, 2000, vol. 41, # 24, p. 4777 - 4780
[3] Patent: WO2005/42514, 2005, A2. Location in patent: Page/Page column 25
[4] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 1, p. 419 - 434
[5] Journal of Organic Chemistry, 1990, vol. 55, # 1, p. 69 - 73

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View Lastest Price from 4-Methoxy-3-pyridinecarboxaldehyde manufacturers

Dideu Industries Group Limited
Product
4-Methoxy-3-pyridinecarboxaldehyde 82257-15-6
Price
US $1.10/g
Min. Order
1g
Purity
99.00%
Supply Ability
100 Tons Min
Release date
2021-10-26
Career Henan Chemical Co
Product
4-Methoxy-3-pyridinecarboxaldehyde 82257-15-6
Price
US $2.00/KG
Min. Order
1KG
Purity
98%MIN
Supply Ability
ASK
Release date
2019-12-25

82257-15-6, 4-Methoxy-3-pyridinecarboxaldehydeRelated Search:


  • 3-Pyridinecarboxaldehyde, 4-methoxy- (9CI)
  • 4-METHOXY-PYRIDINE-3-CARBALDEHYE
  • 4-METHOXYPYRIDINE-3-CARBOXALDEHYDE
  • 4-METHOXY-3-PYRIDINE CARBOXALDEHYDE
  • 3-FORMYL-4-METHOXYPYRIDINE
  • 4-Methoxynicotinaldehyde
  • 4-Methoxypyridine-3-carbaldehyde
  • 4-Methoxy-3-carboxaldehydepyridine
  • 3-Pyridinecarboxaldehyde, 4-Methoxy-
  • 4-MethoxynicotinaL
  • 4-Methoxy-3-pyridinecarboxaldehyde ISO 9001:2015 REACH
  • 82257-15-6
  • Pyridine
  • Pyridines
  • ALDEHYDE
  • Morpholines/Thiomorpholines ,Isoxazoles ,Pyrazoles,Indazoles