5-Bromo-2-fluorobenzaldehyde
Names
[ CAS No. ]:
93777-26-5
[ 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]:
[Related Catalog]:
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
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
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
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)