100047-45-8

Basic information

• Product Name: 2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro- (9CI)
• Synonyms: 2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro- (9CI);4-AMino-1H-pyrrolo[2,3-d]pyriMidin-2(3H)-one;4-aMino-7H-Pyrrolo[2,3-d] pyriMidin-2-ol;4-Amino-1,7-dihydro-2H-pyrrolo[2,3-d]pyrimidin-2-one;4-Amino-1,3-dihydro-2H-pyrrolo[2,3-d]pyrimidin-2-one
• CAS NO: 100047-45-8
• Molecular Formula: C6H6N4O
• Molecular Weight: 150.13804
• Product Categories: PYRIMIDINE;AMINEPRIMARY
• Mol File: 100047-45-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Refractive Index: 1.89
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro- (9CI)(100047-45-8)
• EPA Substance Registry System: 2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro- (9CI)(100047-45-8)

Safety Data

• Hazardous Substances Data: 100047-45-8(Hazardous Substances Data)

Usage

Description

2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro(9CI) is a heterocyclic chemical compound with the molecular formula C6H7N3O. It features a pyrrolopyrimidine ring system and an amino group, which contribute to its potential medicinal properties and applications in pharmaceutical drug development, organic synthesis, and chemical research.

Uses

Used in Pharmaceutical Drug Development:
2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro(9CI) is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its unique structure and functional groups make it a promising candidate for the development of new therapeutic agents with potential applications in treating a range of diseases and medical conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro(9CI) serves as a versatile building block for the creation of more complex organic molecules. Its reactivity and structural features allow for the formation of a wide array of chemical products, making it a valuable component in the synthesis of various organic compounds.
Used in Chemical Research:
2H-Pyrrolo[2,3-d]pyrimidin-2-one, 4-amino-1,7-dihydro(9CI) is also utilized in chemical research to study the properties and reactions of heterocyclic compounds. Its unique structure provides insights into the behavior of similar compounds and contributes to the advancement of knowledge in organic chemistry and related fields.

InChI:InChI=1/C6H6N4O/c7-4-3-1-2-8-5(3)10-6(11)9-4/h1-2H,(H4,7,8,9,10,11)

Upstream product

• 100383-13-9 4-amino-2-methoxy-7H-pyrrolo<2,3-d>pyrimidine 
• 74895-37-7 2-Cyan-4,4-diethoxybuttersaeurenitril 

Relevant articles and documents

Furanoside-Pyranoside Isomerization of Tubercidin and its 2'-Deoxy Derivatives: Influence of Nucleobase and Sugar Structure on the Proton-catalysed Reaction

2'-Deoxy-2-methoxytubercidin (6a) which was prepared from the nucleobase (1a) with the halogenose (2) via phase-transfer glycosylation isomerizes rapidly under acidic conditions.Two pyranosides and the anomeric furanoside (5a) are formed.The isomerization process was followed kinetically, demonstrating that furanoside formation is kinetically controlled whereas the β-pyranoside (7a) is the thermodynamically most stable product.From 2'-deoxytubercidin (6b) similar results were obtained but isomerization was slow, compared with (6a).The ribonucleoside tubercidin (6c) did isomerize only under vigorous acid treatment leading to the α-furanoside (5c) and the nucleobase (1c) by cleavage of the N-glycosylic bond.