32570-17-5

Basic information

• Product Name: 1H-Pyrrole, 1-(2-methoxyphenyl)-2,5-dimethyl-
• CAS NO: 32570-17-5
• Molecular Formula: C13H15NO
• Molecular Weight: 201.268
• Mol File: 32570-17-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole, 1-(2-methoxyphenyl)-2,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole, 1-(2-methoxyphenyl)-2,5-dimethyl-(32570-17-5)
• EPA Substance Registry System: 1H-Pyrrole, 1-(2-methoxyphenyl)-2,5-dimethyl-(32570-17-5)

Safety Data

• Hazardous Substances Data: 32570-17-5(Hazardous Substances Data)

Upstream product

• 60176-18-3 1-(2-iodophenyl)-2,5-dimethyl-1H-pyrrole 
• 124-41-4 sodium methylate 
• 930-87-0 1,2,5-trimethyl-1H-pyrrole 
• 625-84-3 2,5-Dimethylpyrrole 
• 90-04-0 2-methoxy-phenylamine 
• 91-23-6 2-Nitroanisole 
• 110-13-4 2,5-hexanedione 
• 615-43-0 2-iodophenylamine 
• 67-56-1 methanol 

Downstream Products

• 90-04-0 2-methoxy-phenylamine 
• 124678-35-9 N-(2-methoxyphenyl)-2,5-dimethylpyrrole-3-carbaldehyde 

Relevant articles and documents

ORTHO SUBSTITUTED PHENYLPYRAZOLO- AND PHENYLPYRROLO-PYRIDAZINE DERIVATIVES HAVING MULTIMODAL ACTIVITY AGAINST PAIN

The present invention relates to ortho substituted phenylpyrazolo- and pyrrolo-pyridazine derivatives having dual pharmacological activity towards both the α2δ subunit, in particular the α2δ-1 subunit, of the voltage-gated calcium channel and the μ-opioid

Indium-mediated one-pot pyrrole synthesis from nitrobenzenes and 1,4-diketones

One-pot reduction-triggered heterocyclizations of nitrobenzene derivatives with 1,4-diketones were investigated. In the presence of indium/AcOH in toluene at 80 C, reaction of nitrobenzenes with 2,5-hexadione produced moderate to excellent yields (40-98%)

Ullman methoxylation in the presence of a 2,5-dimethylpyrrole-blocked aniline: Preparation of 2-fluoro-4-methoxyaniline [ benzenamine, 2-fluoro-4-methoxy- ]

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