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  • 23316-67-8 , 1-氰基-2,3,5-三苯甲酰基-beta-D-呋喃核糖, CAS:23316-67-8
23316-67-8 , 1-氰基-2,3,5-三苯甲酰基-beta-D-呋喃核糖, CAS:23316-67-8

23316-67-8 , 1-氰基-2,3,5-三苯甲酰基-beta-D-呋喃核糖, CAS:23316-67-8

23316-67-8 ,Tri-O-benzoyl-b-D-ribofuranosyl cyanide,
1-氰基-2,3,5-三苯甲酰基-beta-D-呋喃核糖,
CAS:23316-67-8
C27H21NO7 / 471.46
MFCD00136146

2,3,5-Tri-O-benzoyl-b-D-ribofuranosyl cyanide

1-氰基-2,3,5-三苯甲酰氧基-beta-D-呋喃核糖,

2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide is a synthetic compound used extensively in scientific research. It is a derivative of ribonucleoside; a structural component of RNA (Ribonucleic acid). The compound contains a ribose sugar attached to a cyanide group and three benzoyl groups at positions 2, 3, and 5 of the ribose molecule.

Synthesis and Characterization

2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide can be synthesized by a variety of methods starting from ribose or ribonucleoside. The most common approach is the reaction of ribose with benzoyl chloride in the presence of a base such as pyridine, followed by the addition of cyanide ion. The product is purified through recrystallization or column chromatography. Characterization of the compound can be done using spectroscopic and chromatographic techniques such as NMR, IR, and HPLC.

Analytical Methods

Various techniques have been used to analyze 2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide, including HPLC, UV-visible spectroscopy, and NMR.

Biological Properties

The compound has been shown to have antitumor activity by inhibiting the growth of cancer cells. It has also been found to possess antiviral and antimicrobial properties.

Toxicity and Safety in Scientific Experiments

The compound has been shown to be relatively safe for use in scientific experiments, with low toxicity levels reported in animal studies.

Applications in Scientific Experiments

2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide has a wide range of applications in scientific research. It is used as a precursor in the synthesis of other ribonucleoside analogs used in anticancer and antiviral drug development. It is also used in the study of RNA structure and function and in the development of new gene therapies.

Current State of Research

Research on 2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide is ongoing, with studies focusing on its antitumor activity, mechanism of action, and potential therapeutic applications.

Potential Implications in Various Fields of Research and Industry

The compound has potential implications in various fields of research and industry, including cancer treatment and drug development, RNA structure and function, and gene therapy.

Limitations and Future Directions

Despite its potential, 2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide has several limitations that need to be addressed. For example, its solubility and stability in water need to be improved to increase its effectiveness as a drug. In addition, more research is needed to fully understand its mechanism of action and potential side effects. Future directions for research can include the development of more stable analogs of 2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide and the investigation of its potential use in other diseases such as viral infections and genetic disorders.

In conclusion, 2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide is a promising compound with various applications in scientific research and potential implications in different fields. Future research should address its limitations and explore new directions that could lead to the development of more effective drugs and therapies.

CAS Number23316-67-8
Product Name2,3,5-Tri-O-benzoyl-beta-D-ribofuranosyl cyanide
IUPAC Name(3,4-dibenzoyloxy-5-cyanooxolan-2-yl)methyl benzoate
Molecular FormulaC27H21NO7
Molecular Weight471.46 g/mol
InChIInChI=1S/C27H21NO7/c28-16-21-23(34-26(30)19-12-6-2-7-13-19)24(35-27(31)20-14-8-3-9-15-20)22(33-21)17-32-25(29)18-10-4-1-5-11-18/h1-15,21-24H,17H2
InChI KeyOFMYTVNDIRTGMR-UARRHKHWSA-N
SMILESC1=CC=C(C=C1)C(=O)OCC2C(C(C(O2)C#N)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4
Synonyms2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl Cyanide; 2,5-Anhydro-D-allonoitrile 3,4,6-Tribenzoate; NSC 326632
Canonical SMILESC1=CC=C(C=C1)C(=O)OCC2C(C(C(O2)C#N)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4
Isomeric SMILESC1=CC=C(C=C1)C(=O)OC[C@@H]2[C@H]([C@H]([C@@H](O2)C#N)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4
CAS No: 23316-67-8 MDL No: MFCD00136146 Chemical Formula: C27H21NO7 Molecular Weight: 471.46

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