2-(α-D-Ribofuranosyl)-4-selenazolecarboxamide

Base Information

Chemical Name:2-(α-D-Ribofuranosyl)-4-selenazolecarboxamide
CAS No.:83705-14-0
Molecular Formula:C₉H₁₂N₂O₅Se
Molecular Weight:307.165
Hs Code.:
Mol file:83705-14-0.mol

Synonyms:2-(α-D-Ribofuranosyl)-4-selenazolecarboxamide

Suppliers and Price of 2-(α-D-Ribofuranosyl)-4-selenazolecarboxamide

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
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price

Total 3 raw suppliers

Chemical Property of 2-(α-D-Ribofuranosyl)-4-selenazolecarboxamide

Chemical Property:

Melting Point:204 - 205 °C (ethanol)
PSA：125.90000
LogP:-1.90820

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(α-D-Ribofuranosyl)-4-selenazolecarboxamide

There total 3 articles about 2-(α-D-Ribofuranosyl)-4-selenazolecarboxamide 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: 70.0%

: 83705-12-8
ethyl 2-(2,3,5-tri-O-benzoyl-α-D-ribofuranosyl)selenazole-4-carboxylate

: 83705-14-0
2-α-D-ribofuranosylselenazole-4-carboxamide

Guidance literature:: With ammonia; In methanol; for 48h; Ambient temperature;
DOI:10.1021/jm00357a024

Reference yield:

: 23316-67-8
2,3,5-tri-O-benzoyl-β-D-ribofuranosyl-1-carbonitrile

: 83705-14-0
2-α-D-ribofuranosylselenazole-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / hydrogen selenide, 4-(dimethylamino)pyridine / 20 h / Ambient temperature

2: 1.0 g / acetonitrile / 1 h / Ambient temperature

3: 70 percent / ammonia / methanol / 48 h / Ambient temperature

With dmap; ammonia; hydrogen selenide; In methanol; acetonitrile;
DOI:10.1021/jm00357a024

Reference yield:

: 83705-10-6
2,5-anhydro-3,4,6-tri-O-benzoyl-β-D-allonoselenoamide

: 83705-14-0
2-α-D-ribofuranosylselenazole-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.0 g / acetonitrile / 1 h / Ambient temperature

2: 70 percent / ammonia / methanol / 48 h / Ambient temperature

With ammonia; In methanol; acetonitrile;
DOI:10.1021/jm00357a024