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6-fluoro-9H-purin-2-amine, also known as 6-fluoroadenine, is a purine derivative and a fluorinated analog of adenine with the molecular formula C5H4FN5. It is a chemical compound that plays a significant role in the pharmaceutical and biotechnology industries due to its potential applications in medical research and drug discovery.

34798-94-2

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34798-94-2 Usage

Uses

Used in Pharmaceutical Synthesis:
6-fluoro-9H-purin-2-amine is used as a key intermediate in the synthesis of pharmaceuticals, particularly for the development of antiviral and antineoplastic agents. Its unique chemical properties and potential antitumor and antiviral activities make it a promising candidate for drug development.
Used in Antiviral Applications:
In the antiviral industry, 6-fluoro-9H-purin-2-amine is used as an active pharmaceutical ingredient for the development of antiviral drugs. Its antiviral properties can help in the treatment and prevention of various viral infections.
Used in Antineoplastic Applications:
In the antineoplastic industry, 6-fluoro-9H-purin-2-amine is used as a therapeutic agent for the treatment of cancer. Its antitumor activities can help in inhibiting the growth and progression of cancer cells.
Used in Nucleic Acid Analysis:
6-fluoro-9H-purin-2-amine is used as a fluorescent DNA probe in the field of nucleic acid analysis. Its fluorescent properties allow for the detection and analysis of specific DNA sequences, contributing to advancements in molecular biology and genetic research.
Used in Biotechnology Research:
In the biotechnology industry, 6-fluoro-9H-purin-2-amine is used as a research tool for studying the structure, function, and interactions of nucleic acids and their related proteins. Its potential applications in nucleic acid analysis and as a fluorescent DNA probe make it valuable for various research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 34798-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,9 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34798-94:
(7*3)+(6*4)+(5*7)+(4*9)+(3*8)+(2*9)+(1*4)=162
162 % 10 = 2
So 34798-94-2 is a valid CAS Registry Number.

34798-94-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-7H-purin-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-6-fluorpurin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34798-94-2 SDS

34798-94-2Relevant academic research and scientific papers

ANTI-HEPATITIS B VIRUS AGENT

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Paragraph 0034, (2020/10/09)

PROBLEM TO BE SOLVED: To provide an anti-hepatitis B virus agent and a prophylactic or therapeutic agent for hepatitis B virus-associated diseases, containing a nucleic acid analog as an active ingredient. SOLUTION: The anti-hepatitis B virus agent and pr

Synthesis of some biologically active halogenopurines

Hu, Yu Lin,Liu, Xiang,Lu, Ming,Ge, Qiang,Liu, Xiao Bin

experimental part, p. 429 - 436 (2010/12/29)

A series of some biologically active halogenopurines were synthesized from commercially available guanine (1). The reaction of guanine with acetic anhydride yielded 2,9-diacetylguanine (2-1) by acetylation reaction. Further treatment of 2-1 with POCl3 by PEG-2000 phase transfer catalysis furnished the important compound 3a, then 2-amino-6-halogenopurines (3b-d) were obtained through chlorine-exchange halogenations between KX and 3a by TPPB phase transfer catalyst. Further, 2-halogenopurines (2-2a-d, 4-2a-d, 5a-d) were efficiently prepared from 2-amino-6-substituted purines (1, 3a, 4-1) via a diazotization catalyzed by their corresponding CuX, and some new compounds 2-2a, 2-2c, 2-2d, 4-2c, 4-2d, 5b, 5c and 5d have been discovered. The structures of synthesized compounds were mainly established on the basis of their elemental analysis, 1H NMR, as well as their mass spectral data. All the title compounds were screened for their antifungal activities, and some of the compounds showed promising activity.

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