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5-(CHLOROMETHYL)-2-METHOXYPYRIDINE

CAS No.
101990-70-9
Chemical Name:
5-(CHLOROMETHYL)-2-METHOXYPYRIDINE
Synonyms
2-methoxy-5-chloromethylpyridine;-(CHLOROMETHYL)-2-METHOXYPYRIDINE;5-(CHLOROMETHYL)-2-METHOXYPYRIDINE;5-(ChloroMerthyl)-2-Methoxy pyridine;Pyridine, 5-(chloroMethyl)-2-Methoxy-
CBNumber:
CB42454441
Molecular Formula:
C7H8ClNO
Molecular Weight:
157.6
MDL Number:
MFCD10697570
MOL File:
101990-70-9.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:40
Product description Number Pack Size Price
5-(Chloromethyl)-2-methoxypyridine B419733 50mg $90
5-(Chloromethyl)-2-methoxypyridine B419733 250mg $350
5-(Chloromethyl)-2-methoxypyridine FC139378 2g $250
5-(CHLOROMETHYL)-2-METHOXYPYRIDINE 95.00% HCH0367311 250MG $283.5
5-(Chloromethyl)-2-methoxypyridine FC139378 500mg $90
More product size

5-(CHLOROMETHYL)-2-METHOXYPYRIDINE Properties

Boiling point 236.1±25.0℃ (760 Torr)
Density 1.173±0.06 g/cm3 (20 ºC 760 Torr)
Flash point 96.6±23.2℃
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka 2.62±0.10(Predicted)
Appearance Colorless to light yellow Liquid

SAFETY

Risk and Safety Statements

5-(CHLOROMETHYL)-2-METHOXYPYRIDINE price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B419733 5-(Chloromethyl)-2-methoxypyridine 101990-70-9 50mg $90 2021-12-16 Buy
TRC B419733 5-(Chloromethyl)-2-methoxypyridine 101990-70-9 250mg $350 2021-12-16 Buy
Biosynth Carbosynth FC139378 5-(Chloromethyl)-2-methoxypyridine 101990-70-9 2g $250 2021-12-16 Buy
American Custom Chemicals Corporation HCH0367311 5-(CHLOROMETHYL)-2-METHOXYPYRIDINE 95.00% 101990-70-9 250MG $283.5 2021-12-16 Buy
Biosynth Carbosynth FC139378 5-(Chloromethyl)-2-methoxypyridine 101990-70-9 500mg $90 2021-12-16 Buy
Product number Packaging Price Buy
B419733 50mg $90 Buy
B419733 250mg $350 Buy
FC139378 2g $250 Buy
HCH0367311 250MG $283.5 Buy
FC139378 500mg $90 Buy

5-(CHLOROMETHYL)-2-METHOXYPYRIDINE Chemical Properties,Uses,Production

Uses

5-(Chloromethyl)-2-methoxypyridine is used in preparation of pyrazolopyridine compounds as RET kinase inhibitor for treatment of RET-related diseases.

Synthesis

(6-methoxypyridin-3-yl)methanol

58584-63-7

5-(CHLOROMETHYL)-2-METHOXYPYRIDINE

101990-70-9

(6-Methoxypyridin-3-yl)methanol (2) (537.8 g, 3.86 mol) obtained in Preparation Example 1 was dissolved in dimethylformamide (1.6 L), cooled in an ice bath under nitrogen protection, and thionyl chloride (310 mL, 4.25 mol) was added slowly and dropwise over a period of 1.3 hours. After the dropwise addition, the reaction mixture was continued to be stirred in an ice bath for 1 hour. Subsequently, toluene (5.4 L) and 2N aqueous sodium hydroxide solution (5.4 L) were sequentially added to the reaction mixture at a temperature not exceeding 23 °C. After stirring for about 10 minutes, the aqueous layer was separated and the organic layer was washed with water (2.7 L). The organic layer was concentrated to dryness under reduced pressure, and toluene (1.0 L) was added to the residue for azeotropic distillation, resulting in 618.8 g of the target product, 5-chloromethyl-2-methoxypyridine (3), as a light yellow oil (556.3 g, 91.4% yield). The structure of the product was confirmed by 1H-NMR (CDCl3): δ (ppm) 8.15 (1H, d, J=2.4 Hz), 7.63 (1H, dd, J=2.4 Hz, 8.4 Hz), 6.75 (1H, d, J=8.4 Hz), 4.55 (2H, s), 3.94 (3H, s).

References

[1] Patent: WO2016/33445, 2016, A1. Location in patent: Paragraph 0259
[2] Tetrahedron, 2014, vol. 70, # 40, p. 7207 - 7220
[3] Patent: US2006/235225, 2006, A1. Location in patent: Page/Page column 4
[4] Patent: US2007/49632, 2007, A1. Location in patent: Page/Page column 38
[5] Patent: US2011/224225, 2011, A1. Location in patent: Page/Page column 23

5-(CHLOROMETHYL)-2-METHOXYPYRIDINE Preparation Products And Raw materials

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5-(CHLOROMETHYL)-2-METHOXYPYRIDINE Spectrum

5-(CHLOROMETHYL)-2-METHOXYPYRIDINE 5-(ChloroMerthyl)-2-Methoxy pyridine Pyridine, 5-(chloroMethyl)-2-Methoxy- -(CHLOROMETHYL)-2-METHOXYPYRIDINE 2-methoxy-5-chloromethylpyridine 101990-70-9