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N,1-bis(4-ethylphenyl)-5-oxopyrrolidine-3-carboxamide

Base Information
  • Chemical Name:N,1-bis(4-ethylphenyl)-5-oxopyrrolidine-3-carboxamide
  • CAS No.:6169-73-9
  • Molecular Formula:C9H19NO3
  • Molecular Weight:189.255
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50387414
N,1-bis(4-ethylphenyl)-5-oxopyrrolidine-3-carboxamide

Synonyms:6169-73-9;N,1-bis(4-ethylphenyl)-5-oxopyrrolidine-3-carboxamide;2-amino-6-hydroxy-2,6-dimethylheptanoicacid;CBMicro_002052;Oprea1_542068;DTXSID50387414;SMSF0016315;STK067235;AKOS000340706;AKOS016758218;CB03561;BIM-0002052.P001;SR-01000229748;SR-01000229748-1

Suppliers and Price of N,1-bis(4-ethylphenyl)-5-oxopyrrolidine-3-carboxamide
Supply Marketing:
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
Total 2 raw suppliers
Chemical Property of N,1-bis(4-ethylphenyl)-5-oxopyrrolidine-3-carboxamide
Chemical Property:
  • Vapor Pressure:2.23E-15mmHg at 25°C 
  • Boiling Point:621.7°C at 760 mmHg 
  • Flash Point:329.8°C 
  • Density:1.181g/cm3 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:5
  • Exact Mass:336.183778013
  • Heavy Atom Count:25
  • Complexity:463
Purity/Quality:

98%Min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=CC=C(C=C1)NC(=O)C2CC(=O)N(C2)C3=CC=C(C=C3)CC
Technology Process of N,1-bis(4-ethylphenyl)-5-oxopyrrolidine-3-carboxamide

There total 2 articles about N,1-bis(4-ethylphenyl)-5-oxopyrrolidine-3-carboxamide 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 hydrogenchloride; Heating;
Guidance literature:
Multi-step reaction with 2 steps
1: aq. NaOH
2: aq. HCl / Heating
With hydrogenchloride; sodium hydroxide;
Refernces

Biotransformation of benzoin by Sphingomonas sp. LK11 and ameliorative effects on growth of Cucumis sativus

10.1007/s00203-019-01623-1

The research investigates the biotransformation of benzoin to benzamide by the plant endophyte Sphingomonas sp. LK11 and its effects on the growth and stress tolerance of Cucumis sativus (cucumber). The study found that Sphingomonas sp. LK11 can convert benzoin to benzamide, which acts as an abiotic stress agent when applied to cucumber plants, reducing their agronomic potential. However, when the plants were inoculated with Sphingomonas sp. LK11 along with benzamide, the negative effects were mitigated, and the plants' growth and stress tolerance were improved. The inoculated plants showed higher levels of chlorophyll b and carotenoids, indicating enhanced photosynthetic capacity and stress tolerance. The study also revealed that Sphingomonas sp. LK11 could regulate oxidative stress by reducing the levels of peroxidase, catalase, and glutathione peroxidase in benzamide-treated plants. The findings suggest that Sphingomonas sp. LK11 has potential for plant growth promotion and stress tolerance through its biotransformation capabilities and its ability to modulate plant physiological processes.

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