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)


Product Details

Product Application of 4-Fluorobenzaldehyde CAS#459-57-4

4-Fluorobenzaldehyde (CAS#459-57-4) is a significant organic synthesis intermediate, typically appearing as a colorless to pale yellow liquid with a characteristic aromatic odor. It exhibits the typical chemical properties of an aldehyde, undergoing reactions such as oxidation, reduction, and condensation. The incorporated fluorine atom introduces distinct reactivity, making the compound a unique reactive site in synthetic applications.


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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 

n20/D 1.521(lit.)

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

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, a fluorinated benzaldehyde, exhibits inhibitory activity against mushroom tyrosinase. It serves as a key synthetic intermediate, notably in the preparation of a pyrazolopyridine derivative that acts as a mitogen-activated protein kinase (MAPK) inhibitor. Its broader applications also include the synthesis of various pharmaceutical compounds.

 

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