5-Bromo-2-fluorobenzaldehyde

Names

[ Name ]:
5-Bromo-2-fluorobenzaldehyde

[Synonym ]:
VHR BF EE
3-bromo-6-fluorobenzaldehyde
EINECS 298-056-6
Benzaldehyde, 5-bromo-2-fluoro-
5-bromo-2-florobenzaldehyde
2-Fluoro-5-Bromo benzaldehyde
5-Brom-2-fluorbenzaldehyd
5-Bromo-2-fluorobenzaldehyde
5-bromo-2-fluoro-benzaldehyde
5-Brom-2-fluorbenzolcarbaldehyd
MFCD00070755

Biological Activity

[Description]:

2-Fluoro-5-bromobenzaldehyde 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

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
232.1±20.0 °C at 760 mmHg

[ Melting Point ]:
58-62°C

[ Molecular Formula ]:
C₇H₄BrFO

[ Molecular Weight ]:
203.01

[ Flash Point ]:
94.2±21.8 °C

[ Exact Mass ]:
201.942947

[ PSA ]:
17.07000

[ LogP ]:
2.60

[ Vapour Pressure ]:
0.1±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.585

[ Storage condition ]:
2-8°C

[ Water Solubility ]:
INSOLUBLE

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
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 ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2913000090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

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

Synthesis and SAR of indazole-pyridine based protein kinase B/Akt inhibitors.

Bioorg. Med. Chem. 14(20) , 6832-46, (2006)

A series of heteroaryl-pyridine containing inhibitors of Akt are reported. The synthesis and structure-activity relationships are discussed, leading to the discovery of a indazole-pyridine analogue (K...

Synthesis of 1,6-, 2,7-, 3,8-, and 4,9-isomers of didodecyl[1]benzothieno[3,2-b][1]benzothiophenes.

J. Org. Chem. 78(15) , 7741-8, (2013)

The synthesis of 1,6-, 2,7-, 3,8-, and 4,9-isomers of dibromo- and didodecyl[1]benzothieno[3,2-b][1]benzothiophenes, via the stilbene pathway, is described. Starting from the synthesis of bromo-2-(met...

Synthesis of 5-cyanoindazole and 1-methyl and 1-aryl-5-cyanoindazoles. Halley F and Sava X.

Synth. Commun. 27(7) , 1199-1207, (1997)