84955-38-4

Basic information

• Product Name: 2-amino-7-[(2-hydroxyethoxy)methyl]-1,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one
• Synonyms: 2-amino-7-[(2-hydroxyethoxy)methyl]-7H-pyrrolo[2,3-d]pyrimidin-4-ol; 7H-pyrrolo[2,3-d]pyrimidin-4-ol, 2-amino-7-[(2-hydroxyethoxy)methyl]-
• CAS NO: 84955-38-4
• Molecular Formula: C₉H₁₂N₄O₃
• Molecular Weight: 224.2166
• Mol File: 84955-38-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 495.5°C at 760 mmHg
• Flash Point: 253.4°C
• Density: 1.61g/cm³
• Vapor Pressure: 1.24E-10mmHg at 25°C
• Refractive Index: 1.707
• CAS DataBase Reference: 2-amino-7-[(2-hydroxyethoxy)methyl]-1,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-7-[(2-hydroxyethoxy)methyl]-1,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one(84955-38-4)
• EPA Substance Registry System: 2-amino-7-[(2-hydroxyethoxy)methyl]-1,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one(84955-38-4)

Safety Data

• Hazardous Substances Data: 84955-38-4(Hazardous Substances Data)

Usage

Molecular structure

Pyrrolopyrimidine derivative

Functional groups

Amino group and hydroxyethyl group
Potential medicinal applications
Ability to interact with biological molecules
Therapeutic properties
Requires further research and testing for specific pharmacological effects and potential uses

Upstream product

• 84955-37-3 2-Amino-7-<(2-hydroxyethoxy)methyl>-4-methoxy-7H-pyrrolo<2,3-d>pyrimidin 
• 96446-01-4 Benzoic acid 2-(2-acetylamino-4-oxo-3,4-dihydro-pyrrolo[2,3-d]pyrimidin-7-ylmethoxy)-ethyl ester 
• 96446-02-5 C₂₈H₂₈N₄O₈ 
• 62160-25-2 2-acetamido-3,7-dihydropyrrolo<2,3-d>pyrimidin-4-one 
• 84955-31-7 4-chloro-7H-pyrrolo[2,3-d]pyrimidin-2-amine 
• 84955-32-8 2-amino-4-methoxy-7H-pyrrolo[2,3-d]-pyrimidine 
• 84981-48-6 2-Amino-4-(2-hydroxyethylthio)-7H-pyrrolo<2,3-d>pyrimidin 
• 84955-36-2 7-<(2-Acetoxyethoxy)methyl>-2-amino-4-methoxy-7H-pyrrolo<2,3-d>pyrimidin 
• 7355-55-7 2-amino-3,7-dihydro-4H-pyrrolo[2,3-d]pyrimidin-4-one 

Relevant articles and documents

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A griup of compounds were prepared in which variations of the ring portion of the acyclovir (ACV) structure were made.These modifications included monocyclic (isocytosine, triazole, imidazole), bicyclic (8-azapurine, pyrrolo pyrimidine, pyrazolo3,