1-(2-Bromoethyl)-4-nitrobenzene

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Names

[ CAS No. ]:
5339-26-4

[ Name ]:
1-(2-Bromoethyl)-4-nitrobenzene

[Synonym ]:
1-(2-Bromoethyl)-4-nitrobenzene
β-(p-Nitrophenyl)ethyl bromide
4-(2-bromoethyl)nitrobenzene
4-Nitrophenethyl bromide
Benzene, 1- (2-bromoethyl)-4-nitro-
Benzene, 1-(2-bromoethyl)-4-nitro-
EINECS 226-271-7
MFCD00007386
4-Nitrophenethylbromide
2-(4-Nitrophenyl)ethyl Bromide

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
309.6±17.0 °C at 760 mmHg

[ Melting Point ]:
67-69 °C(lit.)

[ Molecular Formula ]:
C8H8BrNO2

[ Molecular Weight ]:
230.059

[ Flash Point ]:
141.0±20.9 °C

[ Exact Mass ]:
228.973831

[ PSA ]:
45.82000

[ LogP ]:
2.82

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.596

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H317-H319-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Faceshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38;R43

[ Safety Phrases ]:
S26-S36/37

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29049085

Precursor & DownStream

Precursor

  • (2-Bromoethyl)benzene
  • 1-Ethyl-4-nitrobenzene
  • 4-Nitrophenethyl alcohol
  • 4-Nitrophenylacetic acid
  • 2-(4-nitrophenyl)acetyl chloride

DownStream

  • 4-Nitrophenylacetonitrile
  • 4-[2-(benzenesulfonyl)ethyl]aniline
  • Tyramine
  • 4-(4-nitrophenethyl) morpholine
  • 2-(4-Nitrophenyl)ethanesulfonic acid
  • 1-(2-IODO-ETHYL)-4-NITRO-BENZENE
  • p-(2-Bromoethyl)anilineHydrochloride
  • 1,2,3,4-Tetrahydro-6,7-dimethoxy-2-[2-(4-nitrophenyl)ethyl]isoquinoline
  • 4-[2-(3,4-DIHYDRO-6,7-DIMETHOXY-2(1H)-ISOQUINOLINYL)ETHYL]-BENZENAMINE
  • 4-nitrostyrene

Customs

[ HS Code ]: 2904909090

[ Summary ]:
HS:2904909090 sulphonated, nitrated or nitrosated derivatives of hydrocarbons, whether or not halogenated VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

An ensemble of theta class glutathione transferases with novel catalytic properties generated by stochastic recombination of fragments of two mammalian enzymes.

J. Mol. Biol. 318(1) , 59-70, (2002)

The correlation between sequence diversity and enzymatic function was studied in a library of Theta class glutathione transferases (GSTs) obtained by stochastic recombination of fragments of cDNA enco...

Residue 234 in glutathione transferase T1-1 plays a pivotal role in the catalytic activity and the selectivity against alternative substrates.

Biochem. J. 388(Pt 1) , 387-92, (2005)

GST (glutathione transferase) T1-1 plays an important role in the biotransformation of halogenated alkanes, which are used in large quantities as solvents and occur as environmental pollutants. Many r...

A glutathione S-transferase (GST) isozyme from broccoli with significant sequence homology to the mammalian theta-class of GSTs.

Biochim. Biophys. Acta 1205(1) , 29-38, (1994)

A novel glutathione S-transferase (GST) was purified from broccoli (Brassica oleracea var. italica). Partial amino-acid sequencing indicated that the protein shared significant homology with several d...


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Related Compounds

  • 1-(2-Bromoethyl)-4,4-difluoropiperidine hydrobromide
  • 1-(2-Bromoethyl)-4-fluoro-1H-pyrazole
  • 1-(2-Bromoethyl)-4-(difluoromethoxy)benzene
  • 1-(2-Bromoethyl)-4-(4-nitrophenyl)piperazine
  • 1-(2-Bromoethyl)-4-(Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-1H-Pyrazole
  • 1-(2-bromoethyl)-4-methyl-2,3-dihydro-1H-indene