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2-Chloro-5-Methoxynicotinonitrile

CAS No.
74650-73-0
Chemical Name:
2-Chloro-5-Methoxynicotinonitrile
Synonyms
Compound FL0180;2-Chloro-5-Methoxynicotinonitrile;2-chloro-5-methoxypyridine-3-carbonitrile;2-chloro-5-methoxy-3-Pyridinecarbonitrile;3-Pyridinecarbonitrile, 2-chloro-5-methoxy-
CBNumber:
CB72704196
Molecular Formula:
C7H5ClN2O
Molecular Weight:
168.58
MDL Number:
MFCD18255084
MOL File:
74650-73-0.mol
MSDS File:
SDS
Last updated:2026-05-28 05:44:02

2-Chloro-5-Methoxynicotinonitrile Properties

storage temp. under inert gas (nitrogen or Argon) at 2-8°C

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P301+P310
RIDADR  UN2811

2-Chloro-5-Methoxynicotinonitrile price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 113285 2-Chloro-5-methoxynicotinonitrile 74650-73-0 1.00g $925 2026-05-18 Buy
Synthonix C11819 2-Chloro-5-methoxynicotinonitrile 97.0% 74650-73-0 100mg $73 2026-05-06 Buy
Synthonix C11819 2-Chloro-5-methoxynicotinonitrile 97.0% 74650-73-0 250mg $130 2026-05-06 Buy
Synthonix C11819 2-Chloro-5-methoxynicotinonitrile 97.0% 74650-73-0 500mg $240 2026-05-06 Buy
aablocks AA00FWXF 2-chloro-5-methoxynicotinonitrile 95% 74650-73-0 250mg $87 2026-05-28 Buy
Product number Packaging Price Buy
113285 1.00g $925 Buy
C11819 100mg $73 Buy
C11819 250mg $130 Buy
C11819 500mg $240 Buy
AA00FWXF 250mg $87 Buy

2-Chloro-5-Methoxynicotinonitrile Chemical Properties, Uses, Production

Synthesis

2-chloro-5-methoxynicotinamide

74650-72-9

Triphenylphosphine oxide

791-28-6

2-Chloro-5-Methoxynicotinonitrile

74650-73-0

(E) Preparation of 2-chloro-5-methoxynicotinonitrile: To a flame-dried flask under nitrogen atmosphere, triphenylphosphine oxide (12.0 g, 0.04 mol) and dichloromethane (50 mL) were added, and the mixture was cooled to 0°C-4°C. Subsequently, a solution of trifluoromethanesulfonic anhydride (6.75 mL, 0.04 mol) in dichloromethane (80 mL) was added dropwise. After the dropwise addition, stirring of the reaction mixture was continued for 15 minutes. Next, 2-chloro-5-methoxynicotinamide (8.0 g, 0.04 mol) was added in batches over 15 minutes. The reaction mixture was gradually warmed to room temperature and stirred overnight. After completion of the reaction, the mixture was poured into saturated sodium carbonate solution and extracted with chloroform (2×). The organic phases were combined, concentrated and the residue was purified by silica gel column chromatography using chloroform as eluent to give 6.2 g (86% yield) of 2-chloro-5-methoxynicotinonitrile. The product was characterized by 1H NMR (CDCl3): δ 3.9 (3H, s), 7.5 (1H, d, J = 3 Hz), 8.3 (1H, d, J = 3 Hz); IR spectra (nujol): 2250 cm-1.

References

[1] Patent: US4329351, 1982, A
[2] Patent: US4374140, 1983, A

2-Chloro-5-Methoxynicotinonitrile Preparation Products And Raw materials

2-Chloro-5-Methoxynicotinonitrile Suppliers

Global Suppliers ( 25)
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2-chloro-5-methoxy-3-Pyridinecarbonitrile 2-Chloro-5-Methoxynicotinonitrile 2-chloro-5-methoxypyridine-3-carbonitrile 3-Pyridinecarbonitrile, 2-chloro-5-methoxy- Compound FL0180 74650-73-0