5-Amino-n'-(benzyloxy)-1-pentofuranosyl-1h-imidazole-4-carboximidamide

Base Information

Chemical Name:5-Amino-n'-(benzyloxy)-1-pentofuranosyl-1h-imidazole-4-carboximidamide
CAS No.:35966-87-1
Molecular Formula:C16H21N5O5
Molecular Weight:363.373
Hs Code.:
DSSTox Substance ID:DTXSID30498214
NSC Number:136895,127072

Synonyms:35966-87-1;5-amino-n'-(benzyloxy)-1-pentofuranosyl-1h-imidazole-4-carboximidamide;DTXSID30498214;NSC127072;NSC136895;NSC-127072;NSC-136895;35966-90-6

Suppliers and Price of 5-Amino-n'-(benzyloxy)-1-pentofuranosyl-1h-imidazole-4-carboximidamide

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 1 raw suppliers

Chemical Property of 5-Amino-n'-(benzyloxy)-1-pentofuranosyl-1h-imidazole-4-carboximidamide

Chemical Property:

Boiling Point:745.3°Cat760mmHg
Flash Point:404.6°C
Density:1.62g/cm³
XLogP3:-0.1
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:6
Exact Mass:363.15426879
Heavy Atom Count:26
Complexity:490

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CON=C(C2=C(N(C=N2)C3C(C(C(O3)CO)O)O)N)N
Isomeric SMILES:C1=CC=C(C=C1)CO/N=C(/C2=C(N(C=N2)C3C(C(C(O3)CO)O)O)N)\N

Technology Process of 5-Amino-n'-(benzyloxy)-1-pentofuranosyl-1h-imidazole-4-carboximidamide

There total 2 articles about 5-Amino-n'-(benzyloxy)-1-pentofuranosyl-1h-imidazole-4-carboximidamide 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: