5-Bromoindole-3-carboxaldehyde
Names
[ CAS No. ]:
877-03-2
[ Name ]:
5-Bromoindole-3-carboxaldehyde
[Synonym ]:
MFCD00152016
5-Bromo-1H-indole-3-carbaldehyde
5-Bromoindole-3-carboxaldehyde
1H-Indole-3-carboxaldehyde, 5-bromo-
EINECS 212-884-7
Chemical & Physical Properties
[ Density]:
1.7±0.1 g/cm3
[ Boiling Point ]:
395.5±22.0 °C at 760 mmHg
[ Melting Point ]:
204-207 °C(lit.)
[ Molecular Formula ]:
C9H6BrNO
[ Molecular Weight ]:
224.054
[ Flash Point ]:
193.0±22.3 °C
[ Exact Mass ]:
222.963272
[ PSA ]:
32.86000
[ LogP ]:
2.54
[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C
[ Index of Refraction ]:
1.752
[ Storage condition ]:
Room temperature.
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ 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 ]:
2933990090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2933990090
[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
Articles
Eur. J. Med. Chem. 92 , 776-83, (2015)
Streptochlorin, first isolated as a new antibiotic in 1988 from the lipophilic extracts of the mycelium of a Streptomyces sp, is an indole natural products with a variety of biological activities. Bas...
Antibiotic metabolites from a marine pseudomonad.Antimicrob. Agents Chemother. 11(3) , 411-4, (1977)
An antibiotic-producing pseudomonad was isolated from a seawater sample from a La Jolla, Calif., tidepool. The pseudomonad produces two novel antibacterial compounds, 2-n-pentyl-4-quinolinol and 2-n-h...
5,5'-Dibromo-bis(3'-indolyl)methane induces Kruppel-like factor 4 and p21 in colon cancer cells.Mol. Cancer Ther. 7(7) , 2109-20, (2008)
Bis(3'-indolyl)methane (DIM) is a metabolite of the phytochemical indole-3-carbinol, and both compounds exhibit a broad spectrum of anticancer activities. We have developed a series of synthetic symme...