Chemical intermediate

34408-14-5

  • Product Name:8-Chloroadenosine
  • Molecular Formula:C10H12ClN5O4
  • Specifications:99%
  • Molecular Weight:301.689
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Product Details;

CasNo: 34408-14-5

Molecular Formula: C10H12ClN5O4

99% Purity Commercial production 8-Chloroadenosine 34408-14-5 with Cheapest Price

  • Molecular Formula:C10H12ClN5O4
  • Molecular Weight:301.689
  • Vapor Pressure:5.28E-21mmHg at 25°C 
  • Refractive Index:1.912 
  • Boiling Point:707.4 °C at 760 mmHg 
  • Flash Point:381.6 °C 
  • PSA:139.54000 
  • Density:2.19 g/cm3 
  • LogP:-0.74540 

8-CHLOROADENOSINE(Cas 34408-14-5) Usage

General Description

8-Chloroadenosine is a synthetic derivative of adenosine that has been studied for its potential as an anticancer agent. It is a nucleoside analog that has been shown to inhibit the growth of cancer cells by interfering with their DNA and RNA synthesis. 8-Chloroadenosine has also been found to induce apoptosis, or programmed cell death, in cancer cells, making it a promising candidate for chemotherapy treatment. Additionally, it has been investigated for its potential to enhance the effectiveness of other chemotherapy drugs when used in combination. Overall, 8-Chloroadenosine shows promise as a novel therapeutic agent for the treatment of various types of cancer.

InChI:InChI=1/C10H12ClN5O4/c11-10-15-4-7(12)13-2-14-8(4)16(10)9-6(19)5(18)3(1-17)20-9/h2-3,5-6,9,17-19H,1H2,(H2,12,13,14)

34408-14-5 Relevant articles

Studies on nucleosides and nucleotides. LXXIII. Chlorination of adenosine and its N6-methyl derivatives with t-butyl hypochlorite

Ikehara,Ogiso,Maruyama

, p. 575 - 578 (1977)

-

ADENOSINE DERIVATIVES FOR USE IN THE TREATMENT OF CANCER

-

Page/Page column 55; 56, (2018/01/17)

The present invention relates to chemica...

α,β-Methylene-ADP (AOPCP) Derivatives and Analogues: Development of Potent and Selective ecto-5′-Nucleotidase (CD73) Inhibitors

Bhattarai, Sanjay,Freundlieb, Marianne,Pippel, Jan,Meyer, Anne,Abdelrahman, Aliaa,Fiene, Amelie,Lee, Sang-Yong,Zimmermann, Herbert,Yegutkin, Gennady G.,Str?ter, Norbert,El-Tayeb, Ali,Müller, Christa E.

, p. 6248 - 6263 (2015/08/24)

ecto-5′-Nucleotidase (eN, CD73) catalyze...

6,8-DISUBSTITUTED PURINE COMPOSITIONS

-

Paragraph 0127, (2013/03/28)

6,8-Disubstituted purines which can be u...

Synthesis and hybridization properties of RNA containing 8-chloroadenosine.

Chen, Lisa S,Sheppard, Terry L

, p. 599 - 617 (2007/10/03)

8-Chloroadenosine (8-Cl-Ado) has shown p...

34408-14-5 Process route

adenosine
58-61-7

adenosine

8-chloroadenosine
34408-14-5

8-chloroadenosine

Conditions
Conditions Yield
With N-chloro-succinimide; acetic acid; In N,N-dimethyl-formamide; at 20 ℃; for 48h; Concentration; Reagent/catalyst;
52%
With hydrogenchloride; 3-chloro-benzenecarboperoxoic acid; In N,N-dimethyl acetamide; for 3.5h; Ambient temperature;
50%
With hydrogenchloride; 3-chloro-benzenecarboperoxoic acid; In N,N-dimethyl acetamide; at 0 - 25 ℃; for 2.5h;
39%
N<sub>6</sub>-Benzyladenosine
4294-16-0

N6-Benzyladenosine

8-chloroadenosine
34408-14-5

8-chloroadenosine

6-benzylamino-8-chloro-9-(β-D-ribofuranosyl)purine
1427459-38-8

6-benzylamino-8-chloro-9-(β-D-ribofuranosyl)purine

Conditions
Conditions Yield
With N-chloro-succinimide; In N,N-dimethyl-formamide; at 45 ℃; for 18h;
20%

34408-14-5 Upstream products

  • 58-61-7
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    water

  • 4294-16-0
    4294-16-0

    N6-Benzyladenosine

  • 3001-45-4
    3001-45-4

    8-mercaptoadenosine

34408-14-5 Downstream products

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    N6-phenoxyacetyl-8-chloroadenosine

  • 13389-13-4
    13389-13-4

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