2-Bromo-4-methylaniline
2-Bromo-4-methylaniline
  • CAS No.:583-68-6
Other grades of this product :
2-Bromo-4-methylaniline Basic information
Product Name:2-Bromo-4-methylaniline
Synonyms:2-bromo-4-methyl-benzenamin;2-Bromo-4-methylbenzenamine;2-Bromo-4-toluidine;2-bromo-p-toluidin;2-Bromo-4-methylaniline,99% (4-Amino-3-bromtoluol);2-Bromo-p-toluid;4-Amino-3-bromotoluene~2-Bromo-p-toluidine;2-Bromo-4-methylanline
CAS:583-68-6
MF:C7H8BrN
MW:186.05
EINECS:209-515-7
Product Categories:Aromatic Hydrocarbons (substituted) & Derivatives;Anilines, Amides & Amines;Amines;blocks;Bromides;Bromine Compounds
Mol File:583-68-6.mol
2-Bromo-4-methylaniline Chemical Properties
Melting point 14-16 °C (lit.)
Boiling point 240 °C (lit.)
density 1.5 g/mL at 25 °C (lit.)
refractive index n20/D 1.602(lit.)
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Chloroform (Slightly)
form Oil
pka2.97±0.10(Predicted)
color Dark Yellow to Dark Beige
Specific Gravity1.500
Water Solubility Insoluble in water.
BRN 1931711
Stability:Air Sensitive
InChIKeyUVRRJILIXQAAFK-UHFFFAOYSA-N
CAS DataBase Reference583-68-6(CAS DataBase Reference)
NIST Chemistry ReferenceBenzenamine, 2-bromo-4-methyl-(583-68-6)
EPA Substance Registry SystemBenzenamine, 2-bromo-4-methyl- (583-68-6)
Safety Information
Hazard Codes T,Xi,Hazard
Risk Statements 23/24/25-36/37/38-33-20/21/22
Safety Statements 36/37/39-45-26
RIDADR UN 2810 6.1/PG 3
WGK Germany 3
RTECS XU4300000
Hazard Note Irritant/Toxic
TSCA Yes
HazardClass 6.1
PackingGroup III
HS Code 29214300
MSDS Information
ProviderLanguage
4-Amino-3-bromotoluene English
SigmaAldrich English
ACROS English
ALFA English
2-Bromo-4-methylaniline Usage And Synthesis
Chemical Propertiesclear light yellow to brown liquid
Uses2-Bromo-4-methylaniline has been used in the synthesis of iminophosphoranes.
General Description2-Bromo-4-methylaniline participates in palladium catalyzed selective amination of 3-bromoquinoline to yield 3-(2-bromo-4-methylphenylamino) quinoline. It reacts with ethyl and methyl imidazo[1,2-a]pyridine-2-carboxylates in the presence of Me3Al to form amide.

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