289665-56-1

Basic information

• Product Name: 1,4-ANHYDRO-2,5-DIDEOXY-2-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-ARABINO-HEXITOL
• Synonyms: 1,4-ANHYDRO-2,5-DIDEOXY-2-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-ARABINO-HEXITOL
• CAS NO: 289665-56-1
• Molecular Formula: C10H14N2O5
• Molecular Weight: 242.23
• Mol File: 289665-56-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,4-ANHYDRO-2,5-DIDEOXY-2-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-ARABINO-HEXITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-ANHYDRO-2,5-DIDEOXY-2-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-ARABINO-HEXITOL(289665-56-1)
• EPA Substance Registry System: 1,4-ANHYDRO-2,5-DIDEOXY-2-(3,4-DIHYDRO-2,4-DIOXO-1(2H)-PYRIMIDINYL)-D-ARABINO-HEXITOL(289665-56-1)

Safety Data

• Hazardous Substances Data: 289665-56-1(Hazardous Substances Data)

Usage

Chemical structure

A complex chemical compound with a long and intricate name.

Derivative

A derivative of the sugar D-arabino-hexitol.

Rings

Contains a 1,4-anhydro ring and a pyrimidine ring.

Potential applications

Has potential applications in the field of pharmaceuticals and drug development.

Unique structure

Its unique structure and properties make it a potential candidate for pharmaceutical and drug development.

Treatment

May have potential use in the treatment of certain diseases or conditions.

Further research

Further research and testing are needed to fully understand its potential applications.

Upstream product

• 289665-46-9 6-benzoyl-1,2-O-isopropylidene-3-O-tosyl-5-deoxy-α-D-glucofuranose 
• 289665-47-0 Benzoic acid 2-[(2R,3R,4S)-4-hydroxy-3-(toluene-4-sulfonyloxy)-tetrahydro-furan-2-yl]-ethyl ester 
• 75646-85-4 3-p-toluenesulphonate of 1,2-O-isopropylidene-5,6-O-methoxymethylidene-α-D-glucofuranose 
• 2946-01-2 (3aR,5R,6S,6aR)-5-((R)-1,2-dihydroxyethyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-yl 4-methylbenzenesulfonate 
• 43138-33-6 5β-vinyl-4β-tosyl-2α,3α-O-isopropylidene tetrahydrofuran 
• 62102-11-8 5-deoxy-1,2-O-isopropylidene-3-O-p-tolylsulfonyl-α-D-xylo-hexofuranose 
• 66-22-8 uracil 
• 289665-51-6 6-O-benzoyl-5-deoxy-1,4:2,3-dianhydro-D-allitol 

Relevant articles and documents

Novel isonucleoside analogues: synthesis of 2'-deoxy-2'-nucleobase-5'-deoxy-1',4'-anhydro-D-altritol

A new class of isonucleoside analogues with branched-sugar 2'-deoxy-2'-nucleobase-5'-deoxy-1',4'-anhydro-D-altritol (21, 23a-c) has been synthesized from D-glucose in 11 steps. The construction of branched-chain sugars has been carried out by hydroboration-oxidation of a double bond in the corresponding hexose. The key intermediate 12 was synthesized from the branched-chain sugar 11 by the reductive cleavage reaction in the presence of TMSOTf and triethylsilane. A strong solvent effect was observed in the intramolecular nucleophilic substitution of 12. The protic solvent is favorable to form the bicyclic compound 18 by double S(N)2 substitution. The opening reaction of epoxide 17 by nucleobases was achieved regioselectively to give the desired isonucleosides in reasonable yield. Copyright (C) 2000 Elsevier Science Ltd.