2-(Cyclohexylamino)adenosine

Base Information

Chemical Name:2-(Cyclohexylamino)adenosine
CAS No.:53296-12-1
Molecular Formula:C₁₆H₂₄N₆O₄
Molecular Weight:364.404
Hs Code.:
DSSTox Substance ID:DTXSID601309259
ChEMBL ID:CHEMBL1256673
Mol file:53296-12-1.mol

Synonyms:CHEMBL1256673;2-(Cyclohexylamino)adenosine;SCHEMBL5040895;DTXSID601309259;BDBM50472924;53296-12-1

Suppliers and Price of 2-(Cyclohexylamino)adenosine

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 1 raw suppliers

Chemical Property of 2-(Cyclohexylamino)adenosine

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:4
Exact Mass:364.18590327
Heavy Atom Count:26
Complexity:482

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)NC2=NC(=C3C(=N2)N(C=N3)C4C(C(C(O4)CO)O)O)N
Isomeric SMILES:C1CCC(CC1)NC2=NC(=C3C(=N2)N(C=N3)[C@H]4[C@@H]([C@@H]([C@H](O4)CO)O)O)N

Technology Process of 2-(Cyclohexylamino)adenosine

There total 4 articles about 2-(Cyclohexylamino)adenosine 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:

: 2004-07-1
2-Amino-6-chloropurine riboside

: 53296-12-1
2-cyclohexylamino-adenosine

Guidance literature:: Multi-step reaction with 3 steps

1: 56 percent / CuI; I₂; isoamyl nitrite / various solvent(s); tetrahydrofuran / 0.5 h / Heating

2: 94 percent / methanolic ammonia / 18 h / 60 °C

3: 2-methoxy-ethanol / 24 h / 125 °C

With copper(l) iodide; ammonia; iodine; isopentyl nitrite; In tetrahydrofuran; 2-methoxy-ethanol; 1: Iodination / 2: ammoniaolysis / 3: Substitution;
DOI:10.1021/jm000287a

Reference yield:

: 313477-85-9
2-iodo-6-chloro-9-(β-D-ribofuranosyl)purine

: 53296-12-1
2-cyclohexylamino-adenosine

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / methanolic ammonia / 18 h / 60 °C

2: 2-methoxy-ethanol / 24 h / 125 °C

With ammonia; In 2-methoxy-ethanol; 1: ammoniaolysis / 2: Substitution;
DOI:10.1021/jm000287a