2-Aminoformycin

Base Information

Chemical Name:2-Aminoformycin
CAS No.:97782-03-1
Molecular Formula:C₁₀H₁₄N₆O₄
Molecular Weight:282.259
Hs Code.:
DSSTox Substance ID:DTXSID90913655
Wikidata:Q82884314
ChEMBL ID:CHEMBL3144000

Synonyms:2-aminoformycin;5,7-diamino-3-(beta-ribofuranosyl)pyrazolo(4,3-d)pyrimidine

Suppliers and Price of 2-Aminoformycin

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 3 raw suppliers

Chemical Property of 2-Aminoformycin

Chemical Property:

Vapor Pressure:3.54E-17mmHg at 25°C
Boiling Point:638.5°Cat760mmHg
Flash Point:340°C
PSA：85.49000
Density:1.842g/cm³
LogP:1.88480
XLogP3:-2.6
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:2
Exact Mass:282.10765295
Heavy Atom Count:20
Complexity:363

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(C1C(C(C(O1)C2=C3C(=NN2)C(=NC(=N3)N)N)O)O)O
Isomeric SMILES:C([C@@H]1[C@H]([C@H]([C@@H](O1)C2=C3C(=NN2)C(=NC(=N3)N)N)O)O)O

Technology Process of 2-Aminoformycin

There total 1 articles about 2-Aminoformycin 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:

: 80206-18-4
5-amino-3-(β-D-ribofuranosyl)-1H-pyrazolo<4,3-d>pyrimidin-7(6H)-one

: 97782-03-1
5,7-diamino-(3-β-D-ribofuranosyl)pyrazolo<4,3-d>pyrimidine

Guidance literature:: With pyridine; tetraethylammonium chloride; acetic anhydride; N,N-dimethyl-aniline; ammonia ethyl alcohol; trichlorophosphate; Yield given. Multistep reaction;
DOI:10.1021/jm00149a033