4-Fluorobenzaldehyde CAS#459-57-4
CAS Number: 459-57-4
Chemical Formula: C7H5FO
Synonyms:
Paroxetine Impurity 58
4-fluoro-benzaldehyd
Benzaldehyde, p-fluoro-
Appearance:Clear colorless to yellow Liquid
HS Code: 29130000
MOQ (Minimum Order Quantity): 1 FCL (Full Container Load)
4-Fluorobenzaldehyde CAS#459-57-4
4-Fluorobenzaldehyde (CAS#459-57-4) is an important organic synthetic intermediate. It is usually a colorless to pale yellow liquid with a special aromatic smell. It has the typical chemical properties of an aldehyde group and can undergo oxidation, reduction, condensation and other reactions. Due to the presence of fluorine atoms, it possesses some special reactivity and can serve as a unique reactive site in organic synthesis.
Parameters
Melting point | -10 °C (lit.) |
Boiling point | 181 °C/758 mmHg (lit.) |
density | 1.157 g/mL at 25 °C (lit.) |
vapor pressure | 19 hPa (70 °C) |
refractive index | n |
Fp | 134 °F |
storage temp. | Store below +30°C. |
solubility | Chloroform, Methanol |
form | Liquid |
color | Clear colorless to yellow |
Specific Gravity | 1.157 |
Water Solubility | IMMISCIBLE |
Sensitive | Air Sensitive |
BRN | 385857 |
Stability: | Air Sensitive |
InChIKey | UOQXIWFBQSVDPP-UHFFFAOYSA-N |
CAS DataBase Reference | 459-57-4(CAS DataBase Reference) |
NIST Chemistry Reference | Benzaldehyde, 4-fluoro-(459-57-4) |
EPA Substance Registry System | Benzaldehyde, 4-fluoro- (459-57-4) |
Safety Information
Hazard Codes | Xi,F |
Risk Statements | 36/37/38 |
Safety Statements | 26-36-37/39-36/37/39-27 |
RIDADR | UN 1989 3/PG 3 |
WGK Germany | 2 |
F | 9-23 |
Hazard Note | Flammable |
TSCA | T |
HazardClass | 3.2 |
PackingGroup | III |
HS Code | 29130000 |
Product Application of 4-Fluorobenzaldehyde CAS#459-57-4
4-Fluorobenzaldehyde is a fluorinated benzaldehyde with inhibitory activity of mushroom tyrosinase. 4-Fluorobenzaldehyde is used in the preparation of pyrazolopyridine derivative, which finds application as mitogen-activated protein kinase (MAPK) inhibitor. It also serves as a synthetic intermediate in the preparation of pharmaceutical compounds.
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