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3-[(2R,4R)-2-(hydroxymethyl)-4-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)pyrrolidin-1-yl]propanenitrile

Base Information Edit
  • Chemical Name:3-[(2R,4R)-2-(hydroxymethyl)-4-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)pyrrolidin-1-yl]propanenitrile
  • CAS No.:121330-13-0
  • Molecular Formula:C13H18N4O3
  • Molecular Weight:278.311
  • Hs Code.:
  • Mol file:121330-13-0.mol
3-[(2R,4R)-2-(hydroxymethyl)-4-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)pyrrolidin-1-yl]propanenitrile

Synonyms:

Suppliers and Price of 3-[(2R,4R)-2-(hydroxymethyl)-4-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)pyrrolidin-1-yl]propanenitrile
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 3-[(2R,4R)-2-(hydroxymethyl)-4-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)pyrrolidin-1-yl]propanenitrile Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:1.28g/cm3 
Purity/Quality:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

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Technology Process of 3-[(2R,4R)-2-(hydroxymethyl)-4-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)pyrrolidin-1-yl]propanenitrile

There total 6 articles about 3-[(2R,4R)-2-(hydroxymethyl)-4-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)pyrrolidin-1-yl]propanenitrile 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:
In water; 1.) ice-bath, 1 h, 2.) without ice-bath 1 h;
DOI:10.1021/jm00128a015
Guidance literature:
Multi-step reaction with 5 steps
1: 97.3 percent / H2 / 10percent Pd/C / methanol / 16 h / 760 Torr / Ambient temperature
2: 90 percent / benzene; dimethylformamide; diethyl ether / 1.) -15 deg C, 2 h, 2.) 5 deg C, overnight
3: 89 percent / 15 N aq. NH4OH / 16 h / Heating
4: phenol, HBr, acetic acid / 16 h / 90 °C
5: 73.9 percent / H2O / 1.) ice-bath, 1 h, 2.) without ice-bath 1 h
With ammonium hydroxide; hydrogen bromide; hydrogen; acetic acid; phenol; palladium on activated charcoal; In methanol; diethyl ether; water; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00128a015
Guidance literature:
Multi-step reaction with 4 steps
1: 90 percent / benzene; dimethylformamide; diethyl ether / 1.) -15 deg C, 2 h, 2.) 5 deg C, overnight
2: 89 percent / 15 N aq. NH4OH / 16 h / Heating
3: phenol, HBr, acetic acid / 16 h / 90 °C
4: 73.9 percent / H2O / 1.) ice-bath, 1 h, 2.) without ice-bath 1 h
With ammonium hydroxide; hydrogen bromide; acetic acid; phenol; In diethyl ether; water; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00128a015
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