Adenosine, 2-amino-3'-deoxy-

Base Information

Chemical Name:Adenosine, 2-amino-3'-deoxy-
CAS No.:3608-57-9
Molecular Formula:C10H14N6O3
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID50451402
Nikkaji Number:J1.788.618E
Mol file:3608-57-9.mol

Synonyms:3608-57-9;(2R,3R,5S)-2-(2,6-Diamino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3-ol;Adenosine, 2-amino-3'-deoxy-;SCHEMBL3952851;DTXSID50451402;9-(3-Deoxy-beta-D-erythro-pentofuranosyl)-9H-purine-2,6-diamine;(2R,3R,5S)-2-(2,6-diamino-9H-purin-9-yl)-5-(hydroxymethyl)oxolan-3-ol

Suppliers and Price of Adenosine, 2-amino-3'-deoxy-

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 5 raw suppliers

Chemical Property of Adenosine, 2-amino-3'-deoxy-

Chemical Property:

XLogP3:-1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:2
Exact Mass:266.11273833
Heavy Atom Count:19
Complexity:334

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(OC(C1O)N2C=NC3=C(N=C(N=C32)N)N)CO
Isomeric SMILES:C1[C@H](O[C@H]([C@@H]1O)N2C=NC3=C(N=C(N=C32)N)N)CO

Technology Process of Adenosine, 2-amino-3'-deoxy-

There total 1 articles about Adenosine, 2-amino-3'-deoxy- 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:

: 2096-10-8
adenosine-2-amine

: 3608-57-9
9-(3'-deoxy-β-D-erythro-pentofuranosyl)-2,6-diaminopurine

: 4546-70-7
2-amino-2'-deoxyadenosine

Guidance literature:: With 2,2'-azobis(isobutyronitrile); acetoxyisobutyryl bromide; ammonia; tri-n-butyl-tin hydride; Yield given. Multistep reaction. Yields of byproduct given;
DOI:10.1139/v97-092

Reference yield: 43.0%

: 3608-57-9
9-(3'-deoxy-β-D-erythro-pentofuranosyl)-2,6-diaminopurine

: 15386-69-3
(2R,3R,5S)-2-(6-amino-2-fluoro-9H-purin-9-yl)-5-(hydroxymethyl)oxolan-3-ol

: 6-amino-9-(3-deoxy-β-D-erythro-pentofuranosyl)oxopurine

Guidance literature:: With tetrafluoroboric acid; hydrogen fluoride; sodium nitrite; In tetrahydrofuran; at -12 - -10 ℃; for 1h;
DOI:10.1002/1522-2675(200207)85:7<1893::AID-HLCA1893>3.0.CO;2-P

Reference yield:

: 3608-57-9
9-(3'-deoxy-β-D-erythro-pentofuranosyl)-2,6-diaminopurine

: 159217-68-2
N'-(9-{(2R,3R,5S)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-3-hydroxy-tetrahydro-furan-2-yl}-6-oxo-6,9-dihydro-1H-purin-2-yl)-N,N-dimethyl-formamidine

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / adenosine deaminase, phosphate buffer / dimethylsulfoxide; H₂O

2: 92 percent / methanol

3: 87 percent / pyridine

With phosphate buffer; adenosine deaminase; In pyridine; methanol; water; dimethyl sulfoxide;
DOI:10.1080/07328319708006156