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CAS 5135-30-8

:

Adenosine, 5′-(4-methylbenzenesulfonate)

Description:
Adenosine, 5′-(4-methylbenzenesulfonate), also known by its CAS number 5135-30-8, is a chemical compound that combines the nucleoside adenosine with a sulfonate group derived from 4-methylbenzenesulfonic acid. This compound features a purine base (adenine) linked to a ribose sugar, which is then modified by the addition of a sulfonate moiety at the 5' position. The presence of the sulfonate group enhances the solubility of the compound in aqueous solutions, making it useful in various biochemical applications. Adenosine itself plays a crucial role in cellular energy transfer and signaling, while the sulfonate modification can influence its interaction with biological systems. The compound is typically characterized by its molecular weight, solubility properties, and reactivity, particularly in biochemical assays and studies involving nucleoside metabolism. Its unique structure allows it to participate in various chemical reactions, making it a valuable tool in research and pharmaceutical applications.
Formula:C17H19N5O6S
InChI:InChI=1S/C17H19N5O6S/c1-9-2-4-10(5-3-9)29(25,26)27-6-11-13(23)14(24)17(28-11)22-8-21-12-15(18)19-7-20-16(12)22/h2-5,7-8,11,13-14,17,23-24H,6H2,1H3,(H2,18,19,20)/t11-,13-,14-,17-/m1/s1
InChI key:InChIKey=CAXLRAROZXYOHH-LSCFUAHRSA-N
SMILES:O[C@H]1[C@H](N2C=3C(N=C2)=C(N)N=CN3)O[C@H](COS(=O)(=O)C4=CC=C(C)C=C4)[C@H]1O
Synonyms:
  • (3xi)-5'-O-[(4-methylphenyl)sulfonyl]adenosine
  • 5'-O-[(4-methylphenyl)sulfonyl]adenosine
  • 5′-O-Toluenesulfonyladenosine
  • 5′-O-Tosyladenosine
  • Adenosine 5'-Tosylate
  • Adenosine, 5′-(4-methylbenzenesulfonate)
  • Adenosine, 5′-p-toluenesulfonate
  • N~8~-[5-(diethylamino)pentan-2-yl]-3-(3,4,5-trimethoxyphenyl)pyrido[2,3-b]pyrazine-6,8-diamine
  • 5′-Tosyladenosine
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