C26H26N4O10S

Base Information Edit

Chemical Name:C26H26N4O10S
CAS No.:64067-13-6
Molecular Formula:C26H26 N4 O10 S
Molecular Weight:586.579
Hs Code.:
Nikkaji Number:J310.038C
Mol file:64067-13-6.mol

Synonyms:C26H26N4O10S;C26-H26-N4-O10-S;SCHEMBL10667367;(5R)-6beta-[(R)-1-Hydroxyethyl]-3-[[2-[[[(4-nitrophenyl)methoxy]carbonyl]amino]ethyl]thio]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid (4-nitrophenyl)methyl ester

Suppliers and Price of C26H26N4O10S

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

TRC
(5R,6S)-6-[(1R)-1-Hydroxyethyl]-3-[[2-[[[(4-nitrophenyl)methoxy]carbonyl]amino]ethyl]thio]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylicAcid(4-Nitrophenyl)methylEster
5mg
$ 485.00

Total 3 raw suppliers

Chemical Property of C26H26N4O10S Edit

Chemical Property:

Melting Point:184-185 °C
Boiling Point:840.2±65.0 °C(Predicted)
PKA:11.72±0.46(Predicted)
PSA：225.60000
Density:1.52±0.1 g/cm3(Predicted)
LogP:4.21760
XLogP3:3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:12
Exact Mass:586.13696421
Heavy Atom Count:41
Complexity:1040

Purity/Quality:

99.3% ^*data from raw suppliers

(5R,6S)-6-[(1R)-1-Hydroxyethyl]-3-[[2-[[[(4-nitrophenyl)methoxy]carbonyl]amino]ethyl]thio]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylicAcid(4-Nitrophenyl)methylEster ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C1C2CC(=C(N2C1=O)C(=O)OCC3=CC=C(C=C3)[N+](=O)[O-])SCCNC(=O)OCC4=CC=C(C=C4)[N+](=O)[O-])O
Isomeric SMILES:C[C@H]([C@@H]1[C@H]2CC(=C(N2C1=O)C(=O)OCC3=CC=C(C=C3)[N+](=O)[O-])SCCNC(=O)OCC4=CC=C(C=C4)[N+](=O)[O-])O
Uses (5R,6S)-6-[(1R)-1-Hydroxyethyl]-3-[[2-[[[(4-nitrophenyl)methoxy]carbonyl]amino]ethyl]thio]-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic Acid (4-Nitrophenyl)methyl Ester is an intermediate in the synthesis of Thienamycin (T344270). Thienamycin is one of the most potent naturally produced antibiotics known thus far. It has excellent activity against both Gram-positive and Gram-negative bacteria and is resistant to bacterial β-lactamase enzymes.

Technology Process of C26H26N4O10S

There total 80 articles about C26H26N4O10S 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:

Reference yield: 80.0%