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4-Fluorobenzaldehyde

Names

[ CAS No. ]:
459-57-4

[ Name ]:
4-Fluorobenzaldehyde

[Synonym ]:
4-Fluorobenzaldehyde
EINECS 207-293-6
P-FLUORBENZALDEHYDE
p-Fluorobenzaldehyde
p-Fluoro benzaldehyd
4-fluoro-benzaldehyd
4-Fluorbenzaldehyd
Benzaldehyde, 4-fluoro-
p-Fluoro benzaldehyde
4-Fluorbenzolcarbaldehyd
PFAD
para-fluorobenzaldehyde
MFCD00003378
para-fluorobenzadehyde
4-fluoro-benzaldehyde

Biological Activity

[Description]:

p-Fluorobenzenecarboxaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
182.0±13.0 °C at 760 mmHg

[ Melting Point ]:
−10 °C(lit.)

[ Molecular Formula ]:
C7H5FO

[ Molecular Weight ]:
124.11

[ Flash Point ]:
56.7±0.0 °C

[ Exact Mass ]:
124.032440

[ PSA ]:
17.07000

[ LogP ]:
1.51

[ Vapour Pressure ]:
0.8±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.539

[ Water Solubility ]:
IMMISCIBLE

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H226-H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
UN 1989 3/PG 3

[ WGK Germany ]:
2

[ Packaging Group ]:
III

[ Hazard Class ]:
3.2

[ HS Code ]:
2913000090

Synthetic Route

Precursor & DownStream

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

First Novozym 435 lipase-catalyzed Morita-Baylis-Hillman reaction in the presence of amides.

Enzyme Microb. Technol. 84 , 32-40, (2016)

The first Novozym 435 lipase-catalyzed Morita-Baylis-Hillman (MBH) reaction with amides as co-catalyst was realized. Results showed that neither Novozym 435 nor amide can independently catalyze the re...

Synthesis of the highly selective p38 MAPK inhibitor UR-13756 for possible therapeutic use in Werner syndrome.

Future Med. Chem. 2(2) , 193-201, (2010)

UR-13756 is a potent and selective p38 mitogen-activated protein kinase (MAPK) inhibitor, reported to have good bioavailability and pharmacokinetic properties and, thus, is of potential use in the tre...


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Related Compounds

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