((3aR,5R,6S,6aR)-6-Hydroxy-2,2-Dimethyltetrahydrofuro[2,3-D][1,3]Dioxol-5-Yl)Methyl 4-Methylbenzoate

Modify Date: 2025-09-11 07:53:27

((3aR,5R,6S,6aR)-6-Hydroxy-2,2-Dimethyltetrahydrofuro[2,3-D][1,3]Dioxol-5-Yl)Methyl 4-Methylbenzoate Structure
((3aR,5R,6S,6aR)-6-Hydroxy-2,2-Dimethyltetrahydrofuro[2,3-D][1,3]Dioxol-5-Yl)Methyl 4-Methylbenzoate structure
Common Name ((3aR,5R,6S,6aR)-6-Hydroxy-2,2-Dimethyltetrahydrofuro[2,3-D][1,3]Dioxol-5-Yl)Methyl 4-Methylbenzoate
CAS Number 75096-60-5 Molecular Weight 304.38
Density N/A Boiling Point N/A
Molecular Formula C18H24O4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of ((3aR,5R,6S,6aR)-6-Hydroxy-2,2-Dimethyltetrahydrofuro[2,3-D][1,3]Dioxol-5-Yl)Methyl 4-Methylbenzoate


1,2-Di-O-isopropylidene-5-O-(4-methylbenzoyl)-α-D-xylofuranose is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].

 Names

Name 1,2-O-isopropylidene-5-O-(4-toluoyl)-D-xylofuranose
Synonym More Synonyms

  Biological Activity

Description 1,2-Di-O-isopropylidene-5-O-(4-methylbenzoyl)-α-D-xylofuranose is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
Related Catalog
References

[1]. Robak T, Robak P. Purine nucleoside analogs in the treatment of rarer chronic lymphoid leukemias. Curr Pharm Des. 2012;18(23):3373-88.  

 Chemical & Physical Properties

Molecular Formula C18H24O4
Molecular Weight 304.38
Exact Mass 308.12600
PSA 74.22000
LogP 1.38910
InChIKey AFHPWODMQGXJFV-QVHKTLOISA-N
SMILES Cc1ccc(C(=O)OCC2OC3OC(C)(C)OC3C2O)cc1

 Synonyms

1,2-O-Isopropylidene-5-O-(4-toluoyl)-alpha-D-xylofuranose
1,2-O-ISOPROPYLIDENE-5-O-P-TOLUOYL-A-D-XYLOFURANOSE
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