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4-amino-1-(2,5-anhydropentofuranosyl)pyrimidin-2(1H)-one is a chemical compound with the molecular formula C9H10N2O4. It is a modified nucleoside derivative commonly found as a component of nucleic acids in living organisms. 4-amino-1-(2,5-anhydropentofuranosyl)pyrimidin-2(1H)-one plays a crucial role in the synthesis and study of nucleosides and nucleotides, which are essential building blocks for DNA and RNA molecules.
Used in Biochemical Research:
4-amino-1-(2,5-anhydropentofuranosyl)pyrimidin-2(1H)-one is used as a substrate in biochemical research for studying enzymes involved in nucleoside metabolism. Its unique structure allows researchers to investigate the mechanisms and pathways of nucleoside metabolism, contributing to a better understanding of cellular processes and potential therapeutic targets.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-amino-1-(2,5-anhydropentofuranosyl)pyrimidin-2(1H)-one is used as a starting material or intermediate in the development of new drugs and therapeutic agents. Its potential applications target nucleic acid metabolism and function, offering opportunities for the creation of novel treatments for various diseases and conditions.
Used in Nucleic Acid Synthesis:
4-amino-1-(2,5-anhydropentofuranosyl)pyrimidin-2(1H)-one is used as a key component in the synthesis of nucleic acids, such as DNA and RNA. Its incorporation into these molecules allows for the development of modified nucleic acids with specific properties, which can be utilized in various applications, including gene therapy, molecular diagnostics, and the development of new drugs targeting nucleic acid-based processes.

32830-01-6

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32830-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32830-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,3 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32830-01:
(7*3)+(6*2)+(5*8)+(4*3)+(3*0)+(2*0)+(1*1)=86
86 % 10 = 6
So 32830-01-6 is a valid CAS Registry Number.

32830-01-6SDS

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 4-amino-1-(7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl)pyrimidin-2-one

1.2 Other means of identification

Product number -
Other names 2',5'-Anhydroarabinosylcytosine

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:32830-01-6 SDS

32830-01-6Relevant academic research and scientific papers

PREPARATION OF THE 1-(2,5-ANHYDRO-β-D-ARABINOFURANOSYL) DERIVATIVE OF CYTOSINE AND URACIL AND THEIR CLEAVAGE WITH HYDROGEN BROMIDE

Hrebabecky, Hubert,Brokes, Josef,Beranek, Jiri

, p. 2961 - 2968 (2007/10/02)

Anhydronucleoside Ia was prepared from chloroarabinofuranoxylcytosine IIIc or from 2,2'-anhydro-1-(5-chloro-5-deoxy-β-D-arabinofuranosyl)cytosine by the action of a strongly basic ion exchanger.The anhydro derivative IIa was prepared from 2,2'-anhydro-1-(5-chloro-5-deoxy-β-D-arabinofuranosyl)uracil by treatment with aqueous solution of sodium hydroxide.The action of hydrogen bromide in dimethylformamide on 2',5'-anhydronucleosides Ia and IIa leads both to the cleavage of the anhydro bond under formation of the 5'-bromo derivatives IIIa and IVa and to the cleavage of nucleosidic bond.In case of uracil derivative IIa, the α-arabinofuranosyl derivative V was also isolated after preceding acetylation.For unambiguous proof of the structure, an alternative synthesis of compound V was performed.

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