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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, 6-chloro-9-(2-C-methyl-b-D-ribofuranosyl)-

OC[C@H]1O[C@H]([C@]([C@@H]1O)(C)O)n1cnc2c1ncnc2Cl Request for Quotation
Chemical Name: 9H-Purine, 6-chloro-9-(2-C-methyl-b-D-ribofuranosyl)-
CAS Number: 205171-05-7
Product Number: AG0029X4(AGN-PC-0QV1CR)
Synonyms:
MDL No:
Molecular Formula: C11H13ClN4O4
Molecular Weight: 300.6983

Identification/Properties

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


(2R,3R,4R,5R)-2-(6-Chloro-9H-purin-9-yl)-5-(hydroxymethyl)-3-methyltetrahydrofuran-3,4-diol, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure allows for various applications in organic chemistry.One key application of $name$ in chemical synthesis is as a building block in the synthesis of nucleoside analogs. By selectively modifying the hydroxyl and methyl groups present in $name$, chemists can fine-tune the properties of the resulting nucleoside analogs, potentially enhancing their bioactivity or pharmacokinetic profiles. This compound serves as a valuable intermediate in the creation of modified nucleosides that may find applications in drug development or molecular biology research.$name$ can also be utilized as a chiral starting material in asymmetric synthesis. The presence of multiple stereocenters in its structure makes it an attractive candidate for creating enantiomerically pure compounds. Through strategic manipulations of the chiral centers in $name$, chemists can access a variety of enantioenriched molecules with high stereochemical control.Additionally, $name$ can participate in glycosylation reactions to form glycosidic linkages. Its hydroxyl and hydroxymethyl groups make it suitable for bonding with sugar moieties, enabling the construction of complex carbohydrate derivatives. This application is particularly important in the field of carbohydrate chemistry, where precise control over glycosidic bond formation is crucial for designing carbohydrate-based materials or bioactive compounds.