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1,1-dimethyl-5-nitro-3-(2-pyridon-1-yl)indan-2-ol

Base Information
  • Chemical Name:1,1-dimethyl-5-nitro-3-(2-pyridon-1-yl)indan-2-ol
  • CAS No.:131406-69-4
  • Molecular Formula:C16H16N2O4
  • Molecular Weight:300.314
  • Hs Code.:
  • Mol file:131406-69-4.mol
1,1-dimethyl-5-nitro-3-(2-pyridon-1-yl)indan-2-ol

Synonyms:1,1-dimethyl-5-nitro-3-(2-pyridon-1-yl)indan-2-ol

Suppliers and Price of 1,1-dimethyl-5-nitro-3-(2-pyridon-1-yl)indan-2-ol
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1,1-dimethyl-5-nitro-3-(2-pyridon-1-yl)indan-2-ol
Chemical Property:
  • Vapor Pressure:5.59E-12mmHg at 25°C 
  • Boiling Point:528°C at 760 mmHg 
  • Flash Point:273.2°C 
  • PSA:88.05000 
  • Density:1.364g/cm3 
  • LogP:2.52120 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of 1,1-dimethyl-5-nitro-3-(2-pyridon-1-yl)indan-2-ol

There total 5 articles about 1,1-dimethyl-5-nitro-3-(2-pyridon-1-yl)indan-2-ol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With 2-Pyridone; potassium tert-butylate; In dimethyl sulfoxide; for 72h; Ambient temperature;
DOI:10.1021/jm00107a008
Guidance literature:
Multi-step reaction with 4 steps
1: KBH4 / methanol / 1 h / Ambient temperature
2: p-toluenesulfonic acid / toluene / 16 h / Heating
3: m-chloroperbenzoic acid (m-CPBA) / CH2Cl2 / 48 h
4: 42 percent / KO-t-Bu / dimethylsulfoxide / 72 h / Ambient temperature
With potassium borohydride; potassium tert-butylate; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; dimethyl sulfoxide; toluene;
DOI:10.1021/jm00107a008
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