ChemicalBook > CAS DataBase List > N6-BENZYLADENOSINE

N6-BENZYLADENOSINE

Product Name
N6-BENZYLADENOSINE
CAS No.
4294-16-0
Chemical Name
N6-BENZYLADENOSINE
Synonyms
N6-Bn-Ar;NSC 70423;BAP RIBOSE;BAP RIBOSIDE;Benzyladenosine;6-BENZYLADENOSINE;N-Benzyladenosine;N6-BENZYLADENOSINE;ADENOSINE,6N-BENZYL;-2-(6-(Benzylamino)
CBNumber
CB4339416
Molecular Formula
C17H19N5O4
Formula Weight
357.36
MOL File
4294-16-0.mol
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N6-BENZYLADENOSINE Property

Melting point:
184-186 °C
Boiling point:
490.01°C (rough estimate)
Density 
1.1786 (rough estimate)
refractive index 
1.7600 (estimate)
storage temp. 
2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly, Sonicated)
form 
Solid
pka
13.12±0.70(Predicted)
color 
White to Off-White
BRN 
56815
InChIKey
MRPKNNSABYPGBF-LSCFUAHRSA-N
SMILES
OC[C@H]1O[C@@H](N2C3C(=C(N=CN=3)NCC3=CC=CC=C3)N=C2)[C@H](O)[C@@H]1O
CAS DataBase Reference
4294-16-0(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
22-24/25-36-26
WGK Germany 
3
10-23
HS Code 
29349990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TCI Chemical
Product number
B6797
Product name
N6-Benzyladenosine
Packaging
1G
Price
$122
Updated
2025/07/31
TCI Chemical
Product number
B6797
Product name
N6-Benzyladenosine
Packaging
5G
Price
$366
Updated
2025/07/31
Usbiological
Product number
B1077-92A
Product name
N6-Benzyladenosine
Packaging
500mg
Price
$368
Updated
2021/12/16
TRC
Product number
B224615
Product name
N6-BenzylAdenosine
Packaging
5g
Price
$480
Updated
2021/12/16
TRC
Product number
B224615
Product name
N6-BenzylAdenosine
Packaging
2g
Price
$275
Updated
2021/12/16
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N6-BENZYLADENOSINE Chemical Properties,Usage,Production

Chemical Properties

White Solid

Uses

A selective A1 adenosine receptor agonist

Purification Methods

Purify it by recrystallisation from EtOH. It has max 266nm (aqueous EtOH/HCl) and 269 nm (aqueous EtOH/NaOH). [Kissman & Weiss J Org Chem 21 1053 1956, Beilstein 26 III/IV 3682.]

N6-BENZYLADENOSINE Preparation Products And Raw materials

Raw materials

Preparation Products

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N6-BENZYLADENOSINE Suppliers

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View Lastest Price from N6-BENZYLADENOSINE manufacturers

Career Henan Chemical Co
Product
N6-BENZYLADENOSINE 4294-16-0
Price
US $5.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
1ton
Release date
2019-08-05

4294-16-0, N6-BENZYLADENOSINERelated Search:


  • N6-BENZYLADENOSINE
  • BAP RIBOSE
  • 6-BENZYLAMINOPURINE RIBOSE
  • 6-BENZYLAMINOPURINE RIBOSIDE
  • 6-BENZYLADENOSINE
  • N6-BENZYLADENOSINE SELECTIVE A1 ADENOSIN
  • N6-BENZYL-D-ADENOSINE
  • BAP RIBOSIDE
  • 6-Benzylaminopurine riboside, 99+%
  • ADENOSINE,6N-BENZYL
  • 6-BENZYLAMINOPURINE RIBOSIDE (N-6-BENZYLADENOSINE)
  • benzylaminopurine riboside
  • Benzyladenosine
  • N-(Phenylmethyl)adenosine
  • N-Benzyl-9-β-D-ribofuranosyl-9H-purin-6-amine
  • N-Benzyladenosine
  • N6–BENZYLADENOSINE (BAR)
  • 9-(β-D-Ribofuranosyl)-6-benzylaminopurine
  • 6-(BenzylaMino)-9-β-D-ribofuranosylpurine
  • NSC 70423
  • N<sup>6</sup>-Benzyladenosine
  • 6-BenzylaMinopurine Riboside Discontinued see: B224615
  • N6-Bn-Ar
  • N6-Benzyladenosine >=99.0%
  • -2-(6-(Benzylamino)
  • N6-Benzyladenosine, ≥98%
  • Adenosine,N-(phenylmethyl)-
  • N6-BENZYLADENOSINE USP/EP/BP
  • (2R,3R,4S,5R)-2-(6-(Benzylamino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
  • N6-Benzyladenosine,antiviral agent, natural cytokinin nucleoside
  • DNPH1i(N6-benzyladenosine)
  • 4294-16-0
  • 4294-16-6
  • C6H5CH2C11H12N5O4
  • C17H19N5O4
  • Nucleosides
  • Oligonucleotide Synthesis
  • Specialty Synthesis
  • Aromatics
  • Nucleosides
  • Oligonucleotide Synthesis
  • Specialty Synthesis
  • All Inhibitors
  • Bases & Related Reagents
  • Nucleotides
  • Inhibitors