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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)-

1H-Purine-6,8-dione, 7,9-dihydro-

O=c1[nH]c2c([nH]1)nc[nH]c2=O Request for Quotation
Chemical Name: 1H-Purine-6,8-dione, 7,9-dihydro-
CAS Number: 13231-00-0
Product Number: AG0010IO(AGN-PC-0O11G6)
Synonyms:
MDL No:
Molecular Formula: C5H4N4O2
Molecular Weight: 152.1109

Identification/Properties

Computed Properties
Molecular Weight:
152.113g/mol
XLogP3:
-1.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
152.033g/mol
Monoisotopic Mass:
152.033g/mol
Topological Polar Surface Area:
82.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
304
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7H-Purine-6,8-diol, a vital building block in chemical synthesis, plays a crucial role in a wide range of applications. Chemists utilize this compound as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and materials. Its unique molecular structure serves as a versatile starting material for the synthesis of purine derivatives, which are essential components in drug discovery and development. With its ability to undergo diverse chemical transformations, 7H-Purine-6,8-diol enables the creation of novel compounds with potential therapeutic properties. Additionally, this compound serves as a valuable tool in the construction of complex organic molecules, making it a valuable asset in modern synthetic chemistry.