beta-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-phenyl-

Base Information

Chemical Name:beta-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-phenyl-
CAS No.:72758-43-1
Molecular Formula:C16H16N6O4
Molecular Weight:356.336
Hs Code.:
DSSTox Substance ID:DTXSID90223064
Nikkaji Number:J777.948H
Wikidata:Q76155378

Synonyms:BRN 5650652;beta-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-phenyl-;1-(6-Amino-9H-purin-9-yl)-1-deoxy-N-phenyl-beta-D-ribofuranuronamide;72758-43-1;DTXSID90223064;C16H16N6O4;LS-143784;5'-(Phenylamino)-5'-oxo-5'-deoxyadenosine

Suppliers and Price of beta-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-phenyl-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of beta-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-phenyl-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.77g/cm³
XLogP3:0.5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:356.12330301
Heavy Atom Count:26
Complexity:519

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=O)C2C(C(C(O2)N3C=NC4=C(N=CN=C43)N)O)O
Isomeric SMILES:C1=CC=C(C=C1)NC(=O)[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=NC4=C(N=CN=C43)N)O)O

Technology Process of beta-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-phenyl-

There total 5 articles about beta-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N-phenyl- 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: 81.0%

: 72758-39-5
(3aS,4S,6R,6aR)-6-(6-Amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole-4-carboxylic acid phenylamide

: 72758-43-1
adenosine-5'-(N-phenylcarboxamide)

Guidance literature:: With trifluoroacetic acid; at 0 ℃; for 2h;
DOI:10.1021/jm960313y

Reference yield:

: 19234-66-3
2',3'-isopropylideneadenosine-5'-carboxylic acid

: 72758-43-1
adenosine-5'-(N-phenylcarboxamide)

Guidance literature:: Multi-step reaction with 2 steps

1: 68 mg / methanol; dioxane; H₂O; tetrahydrofuran / Ambient temperature

2: 81 percent / aq. CF₃CO₂H / 2 h / 0 °C

With trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; water;
DOI:10.1021/jm960313y

Reference yield:

: 62-53-3
aniline

: 72758-43-1
adenosine-5'-(N-phenylcarboxamide)

Guidance literature:: Multi-step reaction with 2 steps

1: 68 mg / methanol; dioxane; H₂O; tetrahydrofuran / Ambient temperature

2: 81 percent / aq. CF₃CO₂H / 2 h / 0 °C

With trifluoroacetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; water;
DOI:10.1021/jm960313y