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(3S,αR)-3-[[[(E)-Hydroxyimino](4-hydroxyphenyl)acetyl]amino]-α-(4-hydroxyphenyl)-2-oxo-1-azetidineacetic acid

Base Information
  • Chemical Name:(3S,αR)-3-[[[(E)-Hydroxyimino](4-hydroxyphenyl)acetyl]amino]-α-(4-hydroxyphenyl)-2-oxo-1-azetidineacetic acid
  • CAS No.:63598-46-9
  • Molecular Formula:C19H17N3O7
  • Molecular Weight:399.36
  • Hs Code.:
(3S,αR)-3-[[[(E)-Hydroxyimino](4-hydroxyphenyl)acetyl]amino]-α-(4-hydroxyphenyl)-2-oxo-1-azetidineacetic acid

Synonyms:Nocardicin F;3-<2-(4-hydroxyphenyl)-2-(hydroxyimino)acetamido>nocardicinic acid;

Suppliers and Price of (3S,αR)-3-[[[(E)-Hydroxyimino](4-hydroxyphenyl)acetyl]amino]-α-(4-hydroxyphenyl)-2-oxo-1-azetidineacetic acid
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
  • TRC
  • NocardicinF
  • 50mg
  • $ 17600.00
  • Medical Isotopes, Inc.
  • NocardicinF
  • 50 mg
  • $ 17000.00
Total 5 raw suppliers
Chemical Property of (3S,αR)-3-[[[(E)-Hydroxyimino](4-hydroxyphenyl)acetyl]amino]-α-(4-hydroxyphenyl)-2-oxo-1-azetidineacetic acid
Chemical Property:
  • Melting Point:230-231 °C (decomp) 
  • PKA:3.46±0.10(Predicted) 
  • PSA:159.76000 
  • Density:1.57g/cm3 
  • LogP:0.75780 
Purity/Quality:

99% *data from raw suppliers

NocardicinF *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Nocardicin F is a β-lactam antibiotic.
Technology Process of (3S,αR)-3-[[[(E)-Hydroxyimino](4-hydroxyphenyl)acetyl]amino]-α-(4-hydroxyphenyl)-2-oxo-1-azetidineacetic acid

There total 4 articles about (3S,αR)-3-[[[(E)-Hydroxyimino](4-hydroxyphenyl)acetyl]amino]-α-(4-hydroxyphenyl)-2-oxo-1-azetidineacetic acid 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:
Multi-step reaction with 4 steps
1: 84.8 percent / H2 / Pd-C (10percent)
2: 78.1 percent / H2O; pyridine / 1 h / Ambient temperature; pH 9
3: 40 percent / concd. HCl / acetic acid / 0.5 h / 10 °C
4: 1.) PCl5; 2.) N,N-bis(trimethylsilyl)acetamide / 1.) benzene, 0-5 deg C, 1 h; 2.) CH2Cl2, 0-5 deg C, 1 h
With hydrogenchloride; phosphorus pentachloride; hydrogen; N,N-bis(trimethylsilyl)acetamide; palladium on activated charcoal; In pyridine; water; acetic acid;
DOI:10.1248/cpb.35.3979
Guidance literature:
Multi-step reaction with 3 steps
1: 78.1 percent / H2O; pyridine / 1 h / Ambient temperature; pH 9
2: 40 percent / concd. HCl / acetic acid / 0.5 h / 10 °C
3: 1.) PCl5; 2.) N,N-bis(trimethylsilyl)acetamide / 1.) benzene, 0-5 deg C, 1 h; 2.) CH2Cl2, 0-5 deg C, 1 h
With hydrogenchloride; phosphorus pentachloride; N,N-bis(trimethylsilyl)acetamide; In pyridine; water; acetic acid;
DOI:10.1248/cpb.35.3979
Guidance literature:
Multi-step reaction with 2 steps
1: 40 percent / concd. HCl / acetic acid / 0.5 h / 10 °C
2: 1.) PCl5; 2.) N,N-bis(trimethylsilyl)acetamide / 1.) benzene, 0-5 deg C, 1 h; 2.) CH2Cl2, 0-5 deg C, 1 h
With hydrogenchloride; phosphorus pentachloride; N,N-bis(trimethylsilyl)acetamide; In acetic acid;
DOI:10.1248/cpb.35.3979
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