Ethyl (Z)-((1-(N-((p-hydroxyamidino)benzoyl)-L-alanyl)-4-piperidyl)oxy)acetate

Base Information

Chemical Name:Ethyl (Z)-((1-(N-((p-hydroxyamidino)benzoyl)-L-alanyl)-4-piperidyl)oxy)acetate
CAS No.:172927-65-0
Deprecated CAS:178740-39-1
Molecular Formula:C₂₀H₂₈N₄O₆
Molecular Weight:420.466
Hs Code.:
UNII:YUE443B0NF
Wikipedia:Sibrafiban
NCI Thesaurus Code:C152358
ChEMBL ID:CHEMBL435176
Mol file:172927-65-0.mol

Synonyms:((1-(2-((4-(amino(hydroxyimino)methyl)benzoyl)amino)-1-oxopropyl)-4-piperidinyl)oxy)acetic acid ethyl ester;Ro 48-3657;Ro-48-3657;sibrafiban

Suppliers and Price of Ethyl (Z)-((1-(N-((p-hydroxyamidino)benzoyl)-L-alanyl)-4-piperidyl)oxy)acetate

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

American Custom Chemicals Corporation
SIBRAFIBAN 95.00%
5MG
$ 500.59

Total 19 raw suppliers

Chemical Property of Ethyl (Z)-((1-(N-((p-hydroxyamidino)benzoyl)-L-alanyl)-4-piperidyl)oxy)acetate

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：143.55000
Density:1.33g/cm³
LogP:1.49920
XLogP3:1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:9
Exact Mass:420.20088463
Heavy Atom Count:30
Complexity:625

Purity/Quality:

97% ^*data from raw suppliers

SIBRAFIBAN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)COC1CCN(CC1)C(=O)C(C)NC(=O)C2=CC=C(C=C2)C(=NO)N
Isomeric SMILES:CCOC(=O)COC1CCN(CC1)C(=O)[C@H](C)NC(=O)C2=CC=C(C=C2)/C(=N/O)/N
Uses Antithrombotic; fibrinogen receptor antagonist; platelet aggregation inhibitor.

Technology Process of Ethyl (Z)-((1-(N-((p-hydroxyamidino)benzoyl)-L-alanyl)-4-piperidyl)oxy)acetate

There total 10 articles about Ethyl (Z)-((1-(N-((p-hydroxyamidino)benzoyl)-L-alanyl)-4-piperidyl)oxy)acetate 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: 56.0%