56245-02-4

Basic information

• Product Name: Benzene, 1-(2-methylpropoxy)-2-nitro-
• CAS NO: 56245-02-4
• Molecular Formula: C10H13NO3
• Molecular Weight: 195.218
• Mol File: 56245-02-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(2-methylpropoxy)-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(2-methylpropoxy)-2-nitro-(56245-02-4)
• EPA Substance Registry System: Benzene, 1-(2-methylpropoxy)-2-nitro-(56245-02-4)

Safety Data

• Hazardous Substances Data: 56245-02-4(Hazardous Substances Data)

Upstream product

• 78-83-1 2-methyl-propan-1-ol 
• 91-23-6 2-Nitroanisole 
• 78-77-3 Isobutyl bromide 
• 88-75-5 2-hydroxynitrobenzene 
• 824-38-4 potassium 2-nitrophenoxide 

Downstream Products

• 124769-81-9 N-<2-(2-methoxypropoxy)phenyl>thiourea 
• 98772-05-5 1,6-dihydro-2-<2-(2-methylpropoxy)anilino>-6-oxo-5-pyrimidinecarboxylic acid 
• 124769-86-4 ethyl 4-chloro-2-<2-(2-methylpropoxy)anilino>-5-pyrimidinecarboxylate 
• 124769-85-3 1,6-dihydro-1-methyl-2-<2-(2-methylpropoxy)anilino>-6-dioxo-5-pyrimidinecarboxylic acid 
• 124769-88-6 4-methoxy-2-<2-(2-methylpropoxy)anilino>-5-pyrimidineacrboxylic acid 
• 98771-59-6 ethyl 1,6-dihydro-2-[2-(2-methylpropoxy)anilino]-6-oxo-5-pyrimidinecarboxylate 
• 124769-84-2 ethyl 1,6-dihydro-1-methyl-2-<2-(2-methylpropoxy)anilino>-6-oxo-5-pyrimidinecarboxylate 
• 124769-83-1 N-methyl-N'-<2-(2-methylpropoxy)phenyl>quanidine hydroiodide 
• 124769-82-0 S-methyl-N-<2-(2-methylpropoxy)phenyl>isothiourea hydroiodide 
• 124769-87-5 ethyl 4-methoxy-3-<2-(2-methylpropoxy)anilino>-5-pyrimidinecarboxylate hydrochloride 
• 104065-95-4 2-(2-methylpropoxy)benzenamine 

Relevant articles and documents

Boron-Promoted Ether Interchange Reaction: Synthesis of Alkyl Nitroaromatic Ethers from Methoxynitroarenes

The first protocol for boron-promoted ether interchange reaction of methoxynitroarenes was described. A series of methoxynitroarenes and alcohols, including primary, secondary, as well as tertiary alcohols were reacted smoothly in moderate to good yields under the optimized reaction conditions. This protocol constitutes an operationally simple and scalable strategy for the synthesis of alkyl nitroaromatic ethers. Moreover, the new reactivity of boron reagents was discovered.

NOVEL USE OF THIENOPYRIMIDINES

The present invention relates to the use of thienopyrimidine compounds for the production of pharmaceutical compositions for the treatment of inflammatory diseases.