302790-86-9

Basic information

• Product Name: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-IDITOL
• Synonyms: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-IDITOL
• CAS NO: 302790-86-9
• Molecular Formula: C10H14N2O6
• Molecular Weight: 258.229
• Mol File: 302790-86-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-IDITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-IDITOL(302790-86-9)
• EPA Substance Registry System: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-IDITOL(302790-86-9)

Safety Data

• Hazardous Substances Data: 302790-86-9(Hazardous Substances Data)

Usage

Type of compound

Synthetic chemical compound.

Derivation

Derivative of the naturally occurring sugar, iditol.

Structure

Contains a pyrimidine ring structure.

Potential applications

Pharmaceutical and biotechnology industries.

Antiviral properties

Has shown potential as an antiviral agent and has been studied for its ability to inhibit the growth of certain viruses.

Chiral building block

Has been investigated for its potential as a chiral building block in organic synthesis.

Unique characteristic

Unique chemical structure and potential biological activities make APMG an interesting compound for further research and development.

Upstream product

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Relevant articles and documents

Synthesis of 3-deoxy-3-nucleobase-2,5-anhydro-D-mannitol: A novel class of hydroxymethyl-branched isonucleosides

A concise synthesis of 3-deoxy-3-nucleobase-2,5-anhydro-D-mannitol 6(a- d) has been achieved, using the deamination of 2-amino-2-deoxy-D-glucose to construct in one step the sugar skeleton with the desired sense of chirality at each asymmetric center. The selective dibenzoylation of 2,5-anhydro-D- mannitol 9 was investigated, and the key epoxide intermediate 13 was obtained in good yield via an intramolecular Mitsunobu reaction. The process of opening of epoxide 13 by nucleobases appeared to be regioselective. (C) 2000 Elsevier Science Ltd.