6-溴-2-萘甲酸甲酯

BrC₁₀H₆CO₂CH₃

265.10

MFCD00100408

24878396

NA.22

Methyl 6-bromo-2-naphthoate undergoes aromatic Finkelstein reaction followed by hydrolysis to afford 6-iodo-2-naphthoic acid.

Methyl 6-bromo-2-naphthoate may be used to synthesize:

• 6-vinyl-2-naphthalencarbaldehyde
• methyl 6-(3-tert-butyl-4-methoxyphenyl)-2-naphthoate
• methyl 6-[3-tert-butyl-4-[(tert-butyldiethylsilyl)oxy]-phenyl]-2-naphthoate
• methyl 6-[3-(1-adamantyl)-4-[(tert-butyldimethylsilyl)-oxy]phenyl]-2-naphthoate
• methyl 6-[3-(1-adamantyl)-4-[[(2,3-dimethyl-1,3-dioxolan-4-yl)methylloxy]phenyl]-2-naphthoate
• 2-bromo-6-(bromomethyl)naphthalene

100

98%

123-126 ℃ (lit.)

COC(=O)c1ccc2cc(Br)ccc2c1

1S/C12H9BrO2/c1-15-12(14)10-3-2-9-7-11(13)5-4-8(9)6-10/h2-7H,1H3

JEUBRLPXJZOGPX-UHFFFAOYSA-N

5, 25 g in glass bottle

13 - Non Combustible Solids

WGK 3

Eyeshields, Gloves, type N95 (US)