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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)-

1,2-DIDEOXY-D-RIBOFURANOSE

OC[C@H]1OCC[C@@H]1O Request for Quotation
Chemical Name: 1,2-DIDEOXY-D-RIBOFURANOSE
CAS Number: 91547-59-0
Product Number: AG00696I(AGN-PC-3H453D)
Synonyms:
MDL No:
Molecular Formula: C5H10O3
Molecular Weight: 118.1311

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
118.132g/mol
XLogP3:
-0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
118.063g/mol
Monoisotopic Mass:
118.063g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
74.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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


1,2-Dideoxy-D-ribose is a versatile compound used in chemical synthesis as a building block to create various molecules with unique properties. Its unique structure and properties make it useful in a wide range of applications, particularly in the synthesis of pharmaceuticals and bioactive compounds. The absence of a hydroxyl group at the C2 position distinguishes 1,2-Dideoxy-D-ribose from other sugars, providing opportunities for selective modifications and functionalizations.In chemical synthesis, 1,2-Dideoxy-D-ribose is often employed as a starting material for the construction of complex molecules through diverse organic reactions such as nucleophilic substitutions, acylations, and oxidations. Its structural flexibility allows chemists to introduce specific functional groups at different positions, enabling the fine-tuning of desired properties in the final product. Additionally, the presence of a reactive aldehyde group on the sugar moiety offers a point for further derivatization and manipulation in multi-step synthesis pathways.Moreover, 1,2-Dideoxy-D-ribose plays a crucial role in the development of novel drugs, natural product analogs, and carbohydrate-based compounds with potential biological activities. By incorporating this compound into molecular designs, researchers can explore new chemical space and create diverse libraries of compounds for drug discovery and development efforts. The selective modifications possible with 1,2-Dideoxy-D-ribose provide synthetic chemists with a valuable tool for designing and optimizing molecules with improved potency, selectivity, and pharmacokinetic properties.