398117-44-7

Basic information

• Product Name: 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo
• Synonyms: 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo;3-iodo-1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine
• CAS NO: 398117-44-7
• Molecular Formula: C₅H₅IN₆
• Molecular Weight: 276.04
• Mol File: 398117-44-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 648.5±65.0 °C(Predicted)
• Appearance: /
• Density: 2.551±0.06 g/cm3(Predicted)
• PKA: 10.59±0.30(Predicted)
• CAS DataBase Reference: 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo(398117-44-7)
• EPA Substance Registry System: 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo(398117-44-7)

Safety Data

• Hazardous Substances Data: 398117-44-7(Hazardous Substances Data)

Usage

Description

1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo is a chemical compound belonging to the class of pyrazolopyrimidines. It is characterized by the presence of a pyrazolo and pyrimidine ring fused together, with an iodine atom attached at the 3-position. 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo is structurally similar to purin-2,6-diamine, which makes it a valuable analog for various applications in the field of biology and chemistry.

Uses

Used in Biological Research:
1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo is used as a probe and primer in biological research for various applications. Its structural similarity to purin-2,6-diamine allows it to be utilized in the study of nucleic acids, enzymes, and other biomolecules that interact with purine-based compounds. 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo can be employed to investigate the mechanisms of DNA and RNA synthesis, repair, and replication, as well as to develop new strategies for the detection and treatment of genetic disorders and diseases.
Used in Pharmaceutical Development:
Due to its unique chemical structure and properties, 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo can be used as a starting material or intermediate in the synthesis of novel pharmaceutical compounds. It may serve as a potential candidate for the development of new drugs targeting various diseases, including cancer, viral infections, and neurological disorders. 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo's ability to interact with specific biological targets can be exploited to design and optimize therapeutic agents with improved efficacy and selectivity.
Used in Chemical Synthesis:
1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo can also be employed as a versatile building block in the synthesis of various organic compounds. Its unique structural features make it an attractive candidate for the development of new molecules with potential applications in materials science, agrochemistry, and other fields. 1H-Pyrazolo[3,4-d]pyrimidine-4,6-diamine, 3-iodo's reactivity and functional group compatibility can be exploited to create a wide range of novel chemical entities with diverse properties and functions.

Upstream product

• 5413-80-9 2,4-Diamino-7H-pyrazolo<3,4-d>pyrimidine 
• 183274-51-3 6-amino-3-iodo-4-isopropoxy-1H-pyrazolo[3,4-d]pyrimidine 

Downstream Products

• 908143-18-0 3-iodo-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine 

Relevant articles and documents

Pyrazolo[3,4-d]pyrimidine ribonucleosides related to 2-aminoadenosine and isoguanosine: Synthesis, deamination and tautomerism

The syntheses and properties of 8-aza-7-deazapurine (pyrazolo[3,4-d] pyrimidine) ribonucleosides related to 2-aminoadenosine and isoguanosine are described. Glycosylation of 8-aza-7-deazapurine-2,6-diamine 5 with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-d-ribofur

Real-time linear detection probes: sensitive 5'-minor groove binder-containing probes for PCR analysis

Oligonucleotide probes/conjugates are provided along with method for their use in assays to monitor amplification wherein the signal produced does not rely on 5′ nuclease digestion.