302790-81-4

Basic information

• Product Name: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-5-METHYL-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL
• Synonyms: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-5-METHYL-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL
• CAS NO: 302790-81-4
• Molecular Formula: C11H16N2O6
• Molecular Weight: 272.255
• Mol File: 302790-81-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-5-METHYL-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-5-METHYL-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL(302790-81-4)
• EPA Substance Registry System: 2,5-ANHYDRO-3-DEOXY-3-(3,4-DIHYDRO-5-METHYL-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-MANNITOL(302790-81-4)

Safety Data

• Hazardous Substances Data: 302790-81-4(Hazardous Substances Data)

Usage

Molecular structure

A complex structure containing deoxy-mannitol and pyrimidinyl groups, as well as an anhydrous component and a dihydro-methyl-dioxo group.

Deoxy-mannitol

A sugar molecule that lacks one oxygen atom, which may contribute to the compound's unique properties.

Pyrimidinyl group

A nitrogen-containing ring structure that adds complexity to the compound and may be responsible for potential applications in pharmaceuticals.

Anhydrous component

A part of the molecule that lacks water, which may affect the compound's solubility and reactivity.

Dihydro-methyl-dioxo group

A structural feature consisting of a five-membered ring with two oxygen atoms and a methyl group, contributing to the compound's chemical complexity.

Potential applications

The compound may have uses in pharmaceuticals, organic synthesis, and other fields that require unique molecular structures.

Need for further research

To fully understand the properties and potential uses of this compound, additional research and analysis are necessary.

Upstream product

• 196596-85-7 2,5-anhdyro-4-deoxy-4-(thymin-1-yl)-L-mannofuranose dimethyl acetal 
• 65-71-4 thymin 
• 196596-83-5 3-O-p-tolylsulfonyl-2,5-anhydro-L-idofuranose dimethylacetal 
• 171877-92-2 2,5:3,4-dianhydro-L-talofuranose dimethylacetal 
• 91318-12-6 2,5:3,4-dianhydro-1,6-di-O-benzoyl-D-altritol 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 86363-73-7 (2R,3S,4S,5R)-3,4-dihydroxy(tetrahydrofuran-2,5-diyl)bis(methylene) dibenzoate 
• 41107-82-8 2,5-anhydro-D-mannitol 
• 495-75-0 2,5-anhydro-D-mannose 

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.

Stereoselective synthesis of 4-deoxy-4-nucleobase-2,5-anhydro-L-mannitol derivatives

2,5:3,4-Dianhydro-L-talofuranose dimethylacetal 7 was synthesized from D-glucose in 7 steps. A series of 4-deoxy-4-nucleobase-2,5-anhydro-L-mannitols 13-16 were synthesized regioselectively from 7 in good yields. 6-O-p-Tolylsulfonyl-2,5:3,4-dianhydro-L-ta