1-Bromo-2-methyl-3-nitrobenzene

Modify Date: 2024-01-05 18:45:45

1-Bromo-2-methyl-3-nitrobenzene Structure
1-Bromo-2-methyl-3-nitrobenzene structure
Common Name 1-Bromo-2-methyl-3-nitrobenzene
CAS Number 55289-35-5 Molecular Weight 216.03
Density 1.6±0.1 g/cm3 Boiling Point 259.6±20.0 °C at 760 mmHg
Molecular Formula C7H6BrNO2 Melting Point 38-40 °C(lit.)
MSDS Chinese USA Flash Point 110.8±21.8 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of 1-Bromo-2-methyl-3-nitrobenzene


1-Bromo-2-methyl-3-nitrobenzene is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name 2-Bromo-6-nitrotoluene
Synonym More Synonyms

 1-Bromo-2-methyl-3-nitrobenzene Biological Activity

Description 1-Bromo-2-methyl-3-nitrobenzene 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 259.6±20.0 °C at 760 mmHg
Melting Point 38-40 °C(lit.)
Molecular Formula C7H6BrNO2
Molecular Weight 216.03
Flash Point 110.8±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

 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 Xi:Irritant;
Risk Phrases R36/37/38
Safety Phrases S26-S37/39
RIDADR UN 2810 6.1/PG 1
WGK Germany 3
HS Code 2904909090

 Synthetic Route

~92%

1-Bromo-2-methyl-3-nitrobenzene Structure

1-Bromo-2-methy...

CAS#:55289-35-5

Literature: Nicolaou; Snyder, Scott A.; Huang, Xianhai; Simonsen, Klaus B.; Koumbis, Alexandros E.; Bigot, Antony Journal of the American Chemical Society, 2004 , vol. 126, # 32 p. 10162 - 10173

~%

1-Bromo-2-methyl-3-nitrobenzene Structure

1-Bromo-2-methy...

CAS#:55289-35-5

Literature: Recueil des Travaux Chimiques des Pays-Bas, , vol. 53, p. 1011,1016, 1025

~27%

Detail
Literature: Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), , p. 1606 - 1616

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1-Bromo-2-methyl-3-nitrobenzene Structure

1-Bromo-2-methy...

CAS#:55289-35-5

Literature: Canadian Journal of Chemistry, , vol. 40, p. 511 - 517

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1-Bromo-2-methyl-3-nitrobenzene Structure

1-Bromo-2-methy...

CAS#:55289-35-5

Literature: Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), , p. 1606 - 1616

~%

Detail
Literature: Recueil des Travaux Chimiques des Pays-Bas, , vol. 54, p. 235,238 Recueil des Travaux Chimiques des Pays-Bas, , vol. 53, p. 1011,1016, 1025

~%

Detail
Literature: Recueil des Travaux Chimiques des Pays-Bas, , vol. 54, p. 235,238 Recueil des Travaux Chimiques des Pays-Bas, , vol. 53, p. 1011,1016, 1025

~%

Detail
Literature: Recueil des Travaux Chimiques des Pays-Bas, , vol. 54, p. 235,238 Recueil des Travaux Chimiques des Pays-Bas, , vol. 53, p. 1011,1016, 1025

 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%

 Articles2

More Articles
First total synthesis of the neuronal cell protecting carbazole alkaloid carbazomadurin A by sequential transition metal-catalyzed reactions.

Chem. Commun. (Camb.) (10) , 1170-1, (2003)

The highly oxygenated neuronal cell protecting carbazole alkaloid carbazomadurin A was synthesized in nine steps and 11% overall yield from isovanillic acid.

Palladium-catalyzed reactions in the synthesis of 3-and 4-substituted indoles. 2. Total synthesis of the N-acetyl methyl ester of (±)-clavicipitic acids. Harrington PJ, et al.

J. Am. Chem. Soc. 109(14) , 4335-38, (1987)

 Synonyms

2-Bromo-6-nitrotoluene,2-nitro-6-bromotoluene
EINECS 259-566-4
MFCD00009792
1-Bromo-2-methyl-3-nitrobenzene
2-Bromo-6-nitrotoluene
Benzene, 1-bromo-2-methyl-3-nitro-