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N-[(3S)-2-oxopyrrolidin-3-yl]formamide

Base Information Edit
  • Chemical Name:N-[(3S)-2-oxopyrrolidin-3-yl]formamide
  • CAS No.:146679-04-1
  • Molecular Formula:C5H8N2O2
  • Molecular Weight:128.131
  • Hs Code.:
  • European Community (EC) Number:864-300-0
  • Nikkaji Number:J555.962F
  • Mol file:146679-04-1.mol
N-[(3S)-2-oxopyrrolidin-3-yl]formamide

Synonyms:N-[(3S)-2-oxopyrrolidin-3-yl]formamide;146679-04-1;SCHEMBL9197788;AKOS006358416;N-[(3S)-2-Oxopyrrolidin-3beta-yl]formamide;EN300-2971778

Suppliers and Price of N-[(3S)-2-oxopyrrolidin-3-yl]formamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • (S)-N-(2-OXO-3-PYRROLIDINYL)-FORMAMIDE 95.00%
  • 5MG
  • $ 498.86
  • AccelPharmtech
  • (S)-N-(2-oxo-3-pyrrolidinyl)-Formamide 97.00%
  • 25G
  • $ 7320.00
  • AccelPharmtech
  • (S)-N-(2-oxo-3-pyrrolidinyl)-Formamide 97.00%
  • 5G
  • $ 3900.00
  • AccelPharmtech
  • (S)-N-(2-oxo-3-pyrrolidinyl)-Formamide 97.00%
  • 1G
  • $ 2280.00
Total 0 raw suppliers
Chemical Property of N-[(3S)-2-oxopyrrolidin-3-yl]formamide Edit
Chemical Property:
  • PSA:0.00000 
  • LogP:0.00000 
  • XLogP3:-0.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:128.058577502
  • Heavy Atom Count:9
  • Complexity:135
Purity/Quality:

(S)-N-(2-OXO-3-PYRROLIDINYL)-FORMAMIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CNC(=O)C1NC=O
  • Isomeric SMILES:C1CNC(=O)[C@H]1NC=O
Technology Process of N-[(3S)-2-oxopyrrolidin-3-yl]formamide

There total 2 articles about N-[(3S)-2-oxopyrrolidin-3-yl]formamide 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 1,1'-carbonyldiimidazole; Yield given. Multistep reaction; 1.) CH2Cl2, RT, 30 min, 2.) CH2Cl2, RT, 24 h;
DOI:10.1021/jm00063a001
upstream raw materials:

formic acid

(3S)-3-aminopyrrolidin-2-one

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