3,5-Dibromobenzaldehyde
Names
[ CAS No. ]:
56990-02-4
[ Name ]:
3,5-Dibromobenzaldehyde
[Synonym ]:
3,5-Dibrom-benzaldehyd
3,5-di-bromobenzaldehyde
3,5-Dibromobenzaldehyde
3,5-Dibrombenzolcarbaldehyd
3,5-dibrombenzaldehyde
Benzaldehyde, 3,5-dibromo-
3,5-Dibromo-benzaldehyde
MFCD00156887
Chemical & Physical Properties
[ Density]:
2.0±0.1 g/cm3
[ Boiling Point ]:
287.2±20.0 °C at 760 mmHg
[ Melting Point ]:
84-88 °C(lit.)
[ Molecular Formula ]:
C7H4Br2O
[ Molecular Weight ]:
263.914
[ Flash Point ]:
113.5±8.3 °C
[ Exact Mass ]:
261.862885
[ PSA ]:
17.07000
[ LogP ]:
3.34
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.645
[ Water Solubility ]:
insoluble
MSDS
Safety Information
[ Symbol ]:
GHS05
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H314
[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310
[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
[ Hazard Codes ]:
C:Corrosive;
[ Risk Phrases ]:
R34
[ Safety Phrases ]:
S26-S36/37/39-S45
[ RIDADR ]:
UN 3261 8/PG 2
[ WGK Germany ]:
3
[ Hazard Class ]:
8.0
[ 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
Chemistry 19(12) , 3842-5, (2013)
Double-action haloketones: A super silyl group enabled the first highly diastereoselective Mukaiyama aldol reactions of α-chloro- and α-fluoroketones with a wide range of aldehydes, providing anti-β-s...
Aryl urea analogs with broad-spectrum antibacterial activity.Bioorg. Med. Chem. Lett. 14(22) , 5569-72, (2004)
The preparation and evaluation of novel aryl urea analogs as broad-spectrum antibacterial agents is described. Numerous compounds showed low micromolar minimum inhibitory concentrations (MIC) against ...
Synthesis and luminescence characteristics of conjugated dendrimers with 2, 4, 6-triaryl-1, 3, 5-triazine periphery. Kim CK, et al.J. Polym. Sci. A Polym. Chem. 44(1) , 254-263, (2006)