147212-83-7 Usage
Uses
Used in Organic Synthesis:
5-Ethynyl-1-(2’,3’,5’-tri-O-tert-butyldimethylsilyl--D-ribofuranosyl)-imidazo-4-carbonitrile is used as a synthetic building block for the development of complex organic molecules. Its unique structure allows for a wide range of chemical reactions, making it a valuable compound in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Ethynyl-1-(2’,3’,5’-tri-O-tert-butyldimethylsilyl--D-ribofuranosyl)-imidazo-4-carbonitrile is used as a key intermediate in the synthesis of novel drug candidates. Its ability to participate in various chemical reactions enables the creation of new molecules with potential therapeutic properties, contributing to the development of innovative treatments for various diseases.
Used in Agrochemical Industry:
5-Ethynyl-1-(2’,3’,5’-tri-O-tert-butyldimethylsilyl--D-ribofuranosyl)-imidazo-4-carbonitrile is also utilized in the agrochemical industry as a starting material for the synthesis of new pesticides and other crop protection agents. Its unique chemical properties allow for the development of more effective and environmentally friendly products to protect crops from pests and diseases.
Used in Material Science:
In the field of material science, 5-Ethynyl-1-(2’,3’,5’-tri-O-tert-butyldimethylsilyl--D-ribofuranosyl)-imidazo-4-carbonitrile is used as a component in the development of advanced materials with specific properties. Its incorporation into polymers and other materials can lead to the creation of new materials with improved characteristics, such as enhanced stability, durability, or specific interactions with other molecules.
Used in Research and Development:
5-Ethynyl-1-(2’,3’,5’-tri-O-tert-butyldimethylsilyl--D-ribofuranosyl)-imidazo-4-carbonitrile is a valuable compound in research and development laboratories, where it is used to explore new chemical reactions and investigate the properties of novel molecules. Its unique structure and reactivity make it an ideal candidate for studying various aspects of organic chemistry, including reaction mechanisms, stereochemistry, and the development of new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 147212-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,1 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147212-83:
(8*1)+(7*4)+(6*7)+(5*2)+(4*1)+(3*2)+(2*8)+(1*3)=117
117 % 10 = 7
So 147212-83-7 is a valid CAS Registry Number.
147212-83-7Relevant academic research and scientific papers
Minakawa, Noriaki,Matsuda, Akira
, p. 661 - 664 (1992)
3-Deazapurine nucleosides, 3-deazaguanosine (6) 3-deazaguanosine (12) and 3-deazaadenosine (17), were synthesized from 5-ethynyl-1- β-D-ribofuranosylimidazole-4-carboxamide (2) or -4-carbonitrile (13), which were readily obtained from AICA-riboside, via intramolecular ring closure.
Efficient ribosomal peptidyl transfer critically relies on the presence of the ribose 2′-OH at A2451 of 23S rRNA
Erlacher, Matthias D.,Lang, Kathrin,Wotzel, Brigitte,Rieder, Renate,Micura, Ronald,Polacek, Norbert
, p. 4453 - 4459 (2007/10/03)
The ribosomal peptidyl transferase center is a ribozyme catalyzing peptide bond synthesis in all organisms. We applied a novel modified nucleoside interference approach to identify functional groups at 9 universally conserved active site residues. Owing t
Nucleosides and Nucleotides. 116. Convenient Syntheses of 3-Deazaadenosine, 3-Deazaguanosine, and 3-Deazainosine via Ring Closure of 5-Ethynyl-1-β-D-ribofuranosylimidazole-4-carboxamide or -carbonitrile
Minakawa, Noriaki,Matsuda, Akira
, p. 557 - 570 (2007/10/02)
An easy chemical synthesis of 3-deazapurine nucleosides, 3-deazainosine pyridin-4(5H)-one (8)>, 3-deazaguanosine pyridin-4(5H)-one (23)>, and 3-deazaadenosine 4-amino-1-β-D-ribof
