CAS 4121-39-5
:9-(prop-2-en-1-yl)-9H-purin-6-amine
Description:
9-(Prop-2-en-1-yl)-9H-purin-6-amine, also known as 2-propenyl-6-aminopurine, is a purine derivative characterized by its unique structure that includes a purine base with an allyl group at the 9-position and an amino group at the 6-position. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of purines, such as the ability to participate in hydrogen bonding due to the presence of amino and nitrogen atoms in its structure. The compound is of interest in various fields, including biochemistry and pharmacology, due to its potential role as a plant growth regulator and its influence on nucleic acid metabolism. Its reactivity can be attributed to the presence of the double bond in the allyl group, which may allow for further chemical modifications. As with many purine derivatives, it may also exhibit biological activity, making it a subject of research in medicinal chemistry.
Formula:C8H9N5
InChI:InChI=1/C8H9N5/c1-2-3-13-5-12-6-7(9)10-4-11-8(6)13/h2,4-5H,1,3H2,(H2,9,10,11)
SMILES:C=CCn1cnc2c(N)ncnc12
Synonyms:- 9H-Purin-6-amine, 9-(2-propenyl)-
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Found 4 products.
9-(2-Propenyl)adenine
CAS:Controlled Product<p>Applications 9-(2-Propenyl)adenine is an N-substituted purine used in the preparation of mesityl dihydroisoxazolyl homo-N-nucleosides.<br>References Thalassitis, A. et al.: Bioorg. Med. Chem. Lett., 19, 6433 (2009); Chiacchio, U. et al.: Tetrahedron, 60, 441 (2004)<br></p>Formula:C8H9N5Color and Shape:NeatMolecular weight:175.19



