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CAS 3616-24-8

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9-(2-deoxypentofuranosyl)-9H-purin-2-amine

Description:
9-(2-Deoxypentofuranosyl)-9H-purin-2-amine, commonly known as deoxyadenosine, is a nucleoside that plays a crucial role in biochemistry, particularly in the structure of DNA. It consists of a purine base, adenine, linked to a deoxypentofuranose sugar. This compound is characterized by its ability to participate in the formation of nucleic acids, serving as a building block for DNA synthesis. Deoxyadenosine is involved in various metabolic pathways and is essential for cellular processes such as energy transfer and signal transduction. It can exist in different tautomeric forms, which can influence its reactivity and interactions with other biomolecules. The presence of the amino group at the 2-position of the purine ring is significant for its biological activity. In terms of solubility, deoxyadenosine is generally soluble in water, which facilitates its biological functions. Its CAS number, 3616-24-8, is a unique identifier that helps in the cataloging and referencing of this compound in scientific literature and databases.
Formula:C10H13N5O3
InChI:InChI=1/C10H13N5O3/c11-10-12-2-5-9(14-10)15(4-13-5)8-1-6(17)7(3-16)18-8/h2,4,6-8,16-17H,1,3H2,(H2,11,12,14)
SMILES:C1C(C(CO)OC1n1cnc2c[nH]c(=N)nc12)O
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