4-Bromo-2-nitrotoluene

Modify Date: 2024-01-02 20:26:12

4-Bromo-2-nitrotoluene Structure
4-Bromo-2-nitrotoluene structure
Common Name 4-Bromo-2-nitrotoluene
CAS Number 60956-26-5 Molecular Weight 216.03
Density 1.6±0.1 g/cm3 Boiling Point 256.5±0.0 °C at 760 mmHg
Molecular Formula C7H6BrNO2 Melting Point 45-48 °C(lit.)
MSDS Chinese USA Flash Point 112.7±21.8 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 4-Bromo-2-nitrotoluene


4-Bromo-2-nitrotoluene is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 4-Bromo-2-nitrotoluene
Synonym More Synonyms

 4-Bromo-2-nitrotoluene 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

 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

 Safety Information

Symbol GHS07
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%

 Articles6

More 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)

 Synonyms

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
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