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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)-

Adenosine, 2'-deoxy-, monohydrate

OC[C@H]1O[C@H](C[C@@H]1O)n1cnc2c1ncnc2N.O Request for Quotation
Chemical Name: Adenosine, 2'-deoxy-, monohydrate
CAS Number: 16373-93-6
Product Number: AG001UCU(AGN-PC-0O4OCB)
Synonyms:
MDL No:
Molecular Formula: C10H15N5O4
Molecular Weight: 269.2572

Identification/Properties

Properties
MP:
185-187 °C
BP:
627.2°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Refractive Index:
-25.5 ° (C=0.5, H2O)
Solubility:
H2O: soluble50mg/mL, clear, colorless
Computed Properties
Molecular Weight:
269.261g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
2
Exact Mass:
269.112g/mol
Monoisotopic Mass:
269.112g/mol
Topological Polar Surface Area:
120A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
307
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P301+P312
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Adenosine, 2'-deoxy-, hydrate (1:1) is a key chemical compound commonly used in chemical synthesis processes. This particular form of adenosine is important in various applications within the field of organic chemistry, particularly in the synthesis of nucleoside analogs and pharmaceutical compounds. Its hydrate form allows for easier handling and manipulation in laboratory settings.In chemical synthesis, Adenosine, 2'-deoxy-, hydrate (1:1) serves as a building block for creating more complex molecules due to its unique structure and reactivity. Its involvement in nucleoside analog synthesis is particularly crucial for the development of antiviral and anticancer drugs. By utilizing Adenosine, 2'-deoxy-, hydrate (1:1) as a starting material, chemists can modify its structure to design new compounds with specific biological activities.Furthermore, this compound plays a significant role in DNA and RNA research, as it can be incorporated into nucleic acid analogs for studying genetic processes and interactions. Its versatility and compatibility with various reaction conditions make it a valuable tool in the hands of synthetic chemists aiming to explore new chemical entities with potential therapeutic benefits.