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2-Fluoro-4-methoxybenzaldehyde

Names

[ CAS No. ]:
331-64-6

[ Name ]:
2-Fluoro-4-methoxybenzaldehyde

[Synonym ]:
MFCD00236679
2-Fluoro-4-methoxy benzaldehyde
2-FLUORO-4-METHOXYBENZALDHYDE
3-Fluoro-4-formylanisole
2-Ffuoro-4-methoxybenzaldehyde
VHR BF DO1
4-methoxy-2-fluorobenzaldehyde
2-Fluoro-4-methoxybenzaldehyde
o-fluoro-p-methoxybenzaldehyde
2-Fluoro-p-anisaldehyde
fluoro-4-methoxybenzaldehyde
Benzaldehyde, 2-fluoro-4-methoxy-

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
226.5±20.0 °C at 760 mmHg

[ Melting Point ]:
43-48 °C(lit.)

[ Molecular Formula ]:
C8H7FO2

[ Molecular Weight ]:
154.138

[ Flash Point ]:
88.4±16.7 °C

[ Exact Mass ]:
154.043015

[ PSA ]:
26.30000

[ LogP ]:
1.90

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.526

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R22;R36/37/38

[ Safety Phrases ]:
S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2913000090

Synthetic Route

Customs

[ HS Code ]: 2913000090

[ Summary ]:
HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0%

Articles

Chiral building blocks: enantioselective syntheses of benzyloxymethyl phenyl propionic acids.

Molecules 9(6) , 449-58, (2004)

The synthesis of (2S)-2-benzyloxymethyl-3-(2-fluoro-4-methoxyphenyl)- propionic acid, (2S)-2-benzyloxymethyl-3-(2-fluoro-4-methylphenyl)propionic acid and (2S)-2-benzyl-oxymethyl-3-(2,4-dimethylphenyl...

Synthesis, cytotoxic activity and docking studies of new 4-aza-podophyllotoxin derivatives. Hatti I, et al.

Med. Chem. Res. 24(8) , 3305-3313, (2015)

Tyrosine Hydroxylase Inhibitors. Synthesis and Activity of Substituted Aromatic Amino Acids. Saari WS, et al.

J. Med. Chem. 10(6) , 1008-1014, (1967)


More Articles


Related Compounds

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