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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)-

1,3-Propanediol, 2-[2-(2-amino-9H-purin-9-yl)ethyl]-

OCC(CCn1cnc2c1nc(N)nc2)CO Request for Quotation
Chemical Name: 1,3-Propanediol, 2-[2-(2-amino-9H-purin-9-yl)ethyl]-
CAS Number: 104227-86-3
Product Number: AG01CBF2(AGN-PC-0JMLD5)
Synonyms:
MDL No: MFCD00870146
Molecular Formula: C10H15N5O2
Molecular Weight: 237.2584

Identification/Properties

Computed Properties
Molecular Weight:
237.263g/mol
XLogP3:
-1.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
237.123g/mol
Monoisotopic Mass:
237.123g/mol
Topological Polar Surface Area:
110A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
239
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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


2-(2-(2-Amino-9H-purin-9-yl)ethyl)propane-1,3-diol, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a crucial building block in the creation of nucleoside analogs, which are essential in the development of antiviral and anticancer drugs. Its unique structure and functional groups make it an ideal precursor in the synthesis of pharmaceutical compounds that target specific biological pathways. Additionally, $name$ plays a critical role in the production of nucleotide analogs, which are utilized in molecular biology research for nucleic acid labeling and sequencing applications. Overall, the application of 2-(2-(2-Amino-9H-purin-9-yl)ethyl)propane-1,3-diol in chemical synthesis is fundamental in advancing drug discovery and genomic research.