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Catalog Number:
26146
CAS Number:
1500-85-2
6-Amino-7-déazapurine
Purity:
≥ 98 % (HPLC)
Synonym(s):
4-Amino-7 H -pyrrolo[2,3- d ]pyrimidine
Hazmat
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Product Information

6-Amino-7-deazapurine is a versatile compound recognized for its significant role in biochemical research and pharmaceutical applications. This purine analog is particularly valuable in the synthesis of nucleoside analogs and can serve as a building block in the development of antiviral and anticancer agents. Its unique structure allows it to mimic natural nucleobases, making it an essential tool for researchers studying nucleic acid interactions and enzyme mechanisms.

In addition to its applications in drug development, 6-Amino-7-deazapurine has been utilized in the study of metabolic pathways and the design of novel therapeutic agents. Its ability to inhibit specific enzymes involved in nucleotide metabolism positions it as a promising candidate for further exploration in targeted therapies. Researchers and industry professionals can leverage this compound to enhance their studies in molecular biology and medicinal chemistry, ultimately contributing to advancements in healthcare solutions.

Synonyms
4-Amino-7 H -pyrrolo[2,3- d ]pyrimidine
CAS Number
1500-85-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C6H6N4
Molecular Weight
134.14
MDL Number
MFCD01686848
PubChem ID
5359620
Melting Point
255-262 ?C
Appearance
Poudre blanc cassé
Conditions
Conserver à 0-8°C
General Information
Synonyms
4-Amino-7 H -pyrrolo[2,3- d ]pyrimidine
CAS Number
1500-85-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C6H6N4
Molecular Weight
134.14
MDL Number
MFCD01686848
PubChem ID
5359620
Melting Point
255-262 ?C
Appearance
Poudre blanc cassé
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

6-Amino-7-deazapurine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key building block in the synthesis of nucleoside analogs, which are crucial in developing antiviral and anticancer medications.
  • Biochemical Research: It is used in studies related to purine metabolism, helping researchers understand cellular processes and potential therapeutic targets.
  • Genetic Studies: The compound is employed in the design of inhibitors for enzymes involved in DNA and RNA synthesis, providing insights into genetic regulation and expression.
  • Diagnostic Applications: It can be utilized in the development of diagnostic tools for detecting certain diseases, enhancing the accuracy of medical testing.
  • Material Science: 6-Amino-7-deazapurine is explored for its potential in creating novel materials with unique electronic properties, beneficial in the development of advanced technologies.

Citations