N6-Benzyladenosine

Also known as: 6-Benzyladenosine, 6-Benzylaminopurine Ribose, 6-Benzylaminopurine Riboside, BAP Ribose, BAP Riboside, Benzyladenosine, N-Benzyladenosine, N6-Benzyl-D-adenosine, NSC 70423, N-(Phenylmethyl)adenosine, 6-Benzylaminopurine Ribosiden, Adenosine, N-(phenylmethyl)-, Adenosine, N-benzyl-

N6-Benzyladenosine (CAS 4294-16-0) is a compound in the Organic Compounds category listed in the Jingsj chemical database. It has the molecular formula C17H19N5O4 and a molecular weight of 357.364 g/mol. Key properties include a melting point of 184-186 °C, a boiling point of 689.3±65.0 °C at 760 mmHg, a density of 1.6±0.1 g/cm3 and a flash point of 370.7±34.3 °C. No supplier offers are currently listed; request a quote. Record last updated Aug 21, 2026.

CAS No.: 4294-16-0
Jingsj CID: J-11803-6
Molecular Formula: C₁₇H₁₉N₅O₄
Molecular Weight: 357.364 g/mol
Category: Organic Compounds
Last updated: 8/21/2026

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Physicochemical Properties

Melting Point	184-186 °C
Boiling Point	689.3±65.0 °C at 760 mmHg
Density	1.6±0.1 g/cm3
Flash Point	370.7±34.3 °C
Exact Mass	357.143707
PSA	125.55000
LogP	1.04
Vapor Pressure	0.0±2.3 mmHg at 25°C
Refractive Index	1.763

Activity & Biological Data

Additional Information	[1]. Kaminek M, et al. Cytokinin activities of N6-benzyladenosine derivatives hydroxylated on the side-chain phenyl ring. Journal of Plant Growth Regulation. 1987. 6(2):113. [2]. Castiglioni S, et al. N6-isopentenyladenosine and its analogue N6-benzyladenosine induce cell cycle arrest and apoptosis in bladder carcinoma T24 cells. Anticancer Agents Med Chem. 2013 May;13(4):672-8. [3]. Mlejnek P. Caspase inhibition and N6-benzyladenosine-induced apoptosis in HL-60 cells. J Cell Biochem. 2001;83(4):678-89. [4]. Kim YA, et al. Synthesis, biological evaluation and molecular modeling studies of N6-benzyladenosine analogues as potential anti-toxoplasma agents. Biochem Pharmacol. 2007 May 15;73(10):1558-72. [5]. Grimaldi M, et al. NMR for screening and a biochemical assay: Identification of new FPPS inhibitors exerting anticancer activity. Bioorg Chem. 2020 May;98:103449.

Additional Information

[1]. Kaminek M, et al. Cytokinin activities of N6-benzyladenosine derivatives hydroxylated on the side-chain phenyl ring. Journal of Plant Growth Regulation. 1987. 6(2):113. [2]. Castiglioni S, et al. N6-isopentenyladenosine and its analogue N6-benzyladenosine induce cell cycle arrest and apoptosis in bladder carcinoma T24 cells. Anticancer Agents Med Chem. 2013 May;13(4):672-8. [3]. Mlejnek P. Caspase inhibition and N6-benzyladenosine-induced apoptosis in HL-60 cells. J Cell Biochem. 2001;83(4):678-89. [4]. Kim YA, et al. Synthesis, biological evaluation and molecular modeling studies of N6-benzyladenosine analogues as potential anti-toxoplasma agents. Biochem Pharmacol. 2007 May 15;73(10):1558-72. [5]. Grimaldi M, et al. NMR for screening and a biochemical assay: Identification of new FPPS inhibitors exerting anticancer activity. Bioorg Chem. 2020 May;98:103449.

Frequently Asked Questions

What is the CAS number of N6-Benzyladenosine?

The CAS number of N6-Benzyladenosine is 4294-16-0.

What are the molecular formula and molecular weight of N6-Benzyladenosine?

N6-Benzyladenosine has molecular formula C17H19N5O4 and molecular weight 357.364 g/mol.

What are the upstream and downstream products of N6-Benzyladenosine?

For N6-Benzyladenosine, Upstream Products: 6-Chloropurine riboside, Benzylamine, Inosine; Downstream Products: Adenosine, 8-Chloroadenosine, 8-Bromoadenosine.

Data compiled from public chemical databases such as PubChem and supplier catalogs; supplier offers are provided by suppliers.

Last updated: 8/21/2026

How to cite: Jingsj. "N6-Benzyladenosine (CAS 4294-16-0)". Jingsj Chemical Database. https://www.jingsj.com/compound/J-11803-6 (accessed 2026-11-09).

Data for reference only; verify product details with suppliers before purchase.