N6-(4-Hydroxybenzyl)-adenosine

Base Information

Chemical Name:N6-(4-Hydroxybenzyl)-adenosine
CAS No.:110505-75-4
Molecular Formula:C17H19N5O5
Molecular Weight:373.36300
Hs Code.:2934999090
DSSTox Substance ID:DTXSID00440568
Nikkaji Number:J1.004.023J
Wikidata:Q72483320
Metabolomics Workbench ID:127454
ChEMBL ID:CHEMBL224024
Mol file:110505-75-4.mol

Synonyms:N6-(4-hydroxybenzyl)adenosine;T1-11 compound

Suppliers and Price of N6-(4-Hydroxybenzyl)-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
Packaging
price

Matrix Scientific
N6-(4-Hydroxybenzyl)-adenosine 95+%
1g
$ 1647.00

Matrix Scientific
N6-(4-Hydroxybenzyl)-adenosine 95+%
250mg
$ 742.00

Crysdot
N6-(4-Hydroxybenzyl)-adenosine 98+%
100mg
$ 277.00

Crysdot
N6-(4-Hydroxybenzyl)-adenosine 98+%
10mg
$ 49.00

Crysdot
N6-(4-Hydroxybenzyl)-adenosine 98+%
50mg
$ 166.00

ChemScene
N6-(4-Hydroxybenzyl)adenosine 99.66%
100mg
$ 480.00

ChemScene
N6-(4-Hydroxybenzyl)adenosine 99.66%
10mg
$ 84.00

ChemScene
N6-(4-Hydroxybenzyl)adenosine 99.66%
50mg
$ 288.00

Chemenu
N6-(4-Hydroxybenzyl)-adenosine 98%
100mg
$ 262.00

Biosynth Carbosynth
p-Topolin riboside
250 mg
$ 210.00

Total 16 raw suppliers

Chemical Property of N6-(4-Hydroxybenzyl)-adenosine

Chemical Property:

Melting Point:201-204 °C(Solv: methanol (67-56-1); chloroform (67-66-3))
Boiling Point:753.2±70.0 °C(Predicted)
PKA:9.72±0.15(Predicted)
PSA：145.78000
Density:1.71
LogP:-0.17150
Storage Temp.:Hygroscopic, Refrigerator, under inert atmosphere
Solubility.:DMSO (Slightly), Methanol (Slightly, Sonicated)
XLogP3:0.8
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:5
Exact Mass:373.13861872
Heavy Atom Count:27
Complexity:494

Purity/Quality:

97% ^*data from raw suppliers

N6-(4-Hydroxybenzyl)-adenosine 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1CNC2=C3C(=NC=N2)N(C=N3)C4C(C(C(O4)CO)O)O)O
Isomeric SMILES:C1=CC(=CC=C1CNC2=C3C(=NC=N2)N(C=N3)[C@H]4[C@@H]([C@@H]([C@H](O4)CO)O)O)O
Uses N6-(4-Hydroxybenzyl)adenosine is am endogenous compound extracted from G. elata for research interest for its potential sedative and hypnotic activity, as well as a neuroprotective and therapeutic agent for preventing and treating neurodegenerative disease.

Technology Process of N6-(4-Hydroxybenzyl)-adenosine

There total 8 articles about N6-(4-Hydroxybenzyl)-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: 81.0%