4-Bromo-2-nitrotoluene

Names

[ Name ]:
4-Bromo-2-nitrotoluene

[Synonym ]:
Benzene, 4-bromo-1-methyl-2-nitro-
MFCD00041243
2-nitro-4-broMotoluol
4-Bromo-2-nitrotolune
4-Bromo-2-nitrotoluene
2-nitro-4-bromotoluene
4-Bromo-1-methyl-2-nitrobenzene
4-Bromo-2-Nitreotoluene
EINECS 262-536-3
BROMO(4-)-2-NITROTOLUENE
4-bromo-1-methyl-2-nitro-benzene
4-bromo-2-nitro-toluene
4-BROMO-6-NITROTOLUENE
4-bromo-2-nitromethylbenzene
5-Bromo-2-methylnitrobenzene

Biological Activity

[Description]:

4-Bromo-2-nitrotoluene 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

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
256.5±0.0 °C at 760 mmHg

[ Melting Point ]:
45-48 °C(lit.)

[ Molecular Formula ]:
C₇H₆BrNO₂

[ Molecular Weight ]:
216.03

[ Flash Point ]:
112.7±21.8 °C

[ Exact Mass ]:
214.958176

[ PSA ]:
45.82000

[ LogP ]:
2.98

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.593

[ 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 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S36-S36/37/39-S22

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ Packaging Group ]:
I; II; III

[ Hazard Class ]:
6.1

[ HS Code ]:
2904909090

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

Synthesis of (+/-)-eusynstyelamide A.

Org. Lett. 12(11) , 2664-7, (2010)

The synthesis of (+/-)-eusynstyelamide A has been accomplished in six steps in 13% overall yield from 6-bromoindole, methyl glycidate, and Boc-protected agmatine. If oxygen is carefully excluded from ...

Synthetic studies on perophoramidine and the communesins: construction of the vicinal quaternary stereocenters.

J. Org. Chem. 71(23) , 8891-900, (2006)

An efficient synthetic strategy for installation of the two vicinal quaternary carbon centers of the communesins is reported. Key steps include the O-allylation/Claisen rearrangement of spirolactone s...

Synthesis of 4-Bromo-2-chlorotoluene. Xue XM, et al.

Chin. J. Pharm. 37(9) , 588, (2006)

Related Compounds

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