22242-96-2

Basic information

• Product Name: 4-oxo-7-pentofuranosyl-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile
• CAS NO: 22242-96-2
• Molecular Formula: C₁₂H₁₂N₄O₅
• Molecular Weight: 292.2475
• Mol File: 22242-96-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 724.3°C at 760 mmHg
• Flash Point: 391.8°C
• Density: 1.91g/cm³
• Vapor Pressure: 5.1E-22mmHg at 25°C
• Refractive Index: 1.827
• CAS DataBase Reference: 4-oxo-7-pentofuranosyl-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-oxo-7-pentofuranosyl-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile(22242-96-2)
• EPA Substance Registry System: 4-oxo-7-pentofuranosyl-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile(22242-96-2)

Safety Data

• Hazardous Substances Data: 22242-96-2(Hazardous Substances Data)

Upstream product

• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 123148-78-7 4-chloro-5-iodo-7H-pyrrolo[2,3-d]pyrimidine 
• 480439-89-2 4-chloro-5-iodo-7-[(2,3,5-tri-O-benzoyl)-β-D-ribofuranosyl]-7H-pyrrolo[2,3-d]pyrimidine 
• 952429-18-4 3,7-dihydro-5-iodo-7-(β-D-ribofuranosyl)-4H-pyrrolo[2,3-d]pyrimidin-4-one 
• 606-58-6 Vengicide 

Downstream Products

• 22242-94-0 5-Carboxamido-4-hydroxy-7-(β-D-ribofuranosyl)pyrrolo<2,3-d>pyrimidin 
• 22242-95-1 4-oxo-7-β-D-ribofuranosyl-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidine-5-carbothioic acid amide 
• 52443-16-0 4-chloro-7-(β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carbonitrile 
• 51112-63-1 4-methylthio-7-(β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carbonitrile 
• 57071-71-3 4-methoxy-7-(β-D-ribofuranosyl)pyrrolo[2,3-d]pyrimidine-5-carbonitrile 
• 22242-93-9 7-(β-D-ribofuranosyl)pyrrolo[2,3-d]-4-pyrimidone-5-carboxamidine 

Relevant articles and documents

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The invention relates to a synthetic method of jjar mycin. The technical problems of long steps and high cost of the existing synthesis method are mainly solved. The synthesis method comprises the following synthesis steps: generating a compound 1 from 4-

Pyrrolopyrimidine nucleosides. V. A study on the relative chemical reactivity of the 5-cyano group of the nucleoside antibiotic toyocamycin and desaminotoyocamycin. The synthesis of analogs of sangivamycin.

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