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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

9H-Purine-9-ethanol, 6-amino-a-methyl-, (aR)-

C[C@H](Cn1cnc2c1ncnc2N)O Request for Quotation
Chemical Name: 9H-Purine-9-ethanol, 6-amino-a-methyl-, (aR)-
CAS Number: 14047-28-0
Product Number: AG001CIK(AGN-PC-0PPPGF)
Synonyms:
MDL No: MFCD07369451
Molecular Formula: C8H11N5O
Molecular Weight: 193.2058

Identification/Properties

Properties
MP:
193 °C
BP:
457.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
193.21g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
193.096g/mol
Monoisotopic Mass:
193.096g/mol
Topological Polar Surface Area:
89.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
202
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-9-(2-Hydroxypropyl)adenine, also known as (R)-HPA, plays a crucial role in chemical synthesis as a versatile building block. Its chiral nature makes it particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. By serving as a key intermediate, (R)-HPA enables the creation of complex molecules with precise stereochemistry, leading to enhanced biological activity and therapeutic efficacy in drug development. Its incorporation in synthetic pathways allows for the controlled introduction of functional groups and substitution patterns, affording chemists greater control over the molecular structure and properties of the final compounds. Additionally, the presence of the adenine moiety in (R)-HPA offers opportunities for further diversification through selective derivatization reactions, expanding the scope of its applications in organic synthesis. Overall, (R)-9-(2-Hydroxypropyl)adenine stands as a valuable tool for chemists seeking to design and construct novel molecules with tailored functionalities and improved pharmacological profiles.