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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)-

b-D-Ribofuranuronamide,1-[6-[[(4-aminophenyl)methyl]amino]-9H-purin-9-yl]-1-deoxy-N-methyl-

CNC(=O)[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cnc2c1ncnc2NCc1ccc(cc1)N Request for Quotation
Chemical Name: b-D-Ribofuranuronamide,1-[6-[[(4-aminophenyl)methyl]amino]-9H-purin-9-yl]-1-deoxy-N-methyl-
CAS Number: 152918-26-8
Product Number: AG00ABMS(AGN-PC-0Q6ER4)
Synonyms:
MDL No:
Molecular Formula: C18H21N7O4
Molecular Weight: 399.4038

Identification/Properties

Properties
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
399.411g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
5
Exact Mass:
399.166g/mol
Monoisotopic Mass:
399.166g/mol
Topological Polar Surface Area:
160A^2
Heavy Atom Count:
29
Formal Charge:
0
Complexity:
576
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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


AB-MECA, also known as 1-deoxy-1-[6-[[(3-iodophenyl)methyl]amino]-9H-purin-9-yl]-N-methyl-β-D-ribofuranuronamide, is a powerful chemical compound widely utilized in chemical synthesis. Its unique structure and properties make it a valuable tool in organic chemistry research and application.In chemical synthesis, AB-MECA serves as an important reagent for the introduction of functional groups or modifications in organic molecules. Due to its high reactivity and specificity, AB-MECA can be used to selectively modify certain parts of a molecule while leaving other regions untouched. This precision is crucial in designing and synthesizing complex organic compounds with specific properties and functions.AB-MECA is commonly employed in the synthesis of nucleoside analogues, which are essential building blocks in the development of antiviral and anticancer drugs. Its ability to introduce modified nucleobases into nucleosides allows for the creation of novel compounds with improved pharmacological properties.Furthermore, AB-MECA plays a key role in the preparation of radiolabeled compounds for use in molecular imaging and diagnostic techniques. By incorporating radioactive isotopes into organic molecules using AB-MECA, researchers can track the distribution and metabolism of these compounds in biological systems, enabling a better understanding of disease processes and drug interactions.Overall, the versatile application of AB-MECA in chemical synthesis makes it a valuable asset for chemists and researchers seeking to explore new avenues in drug discovery, molecular imaging, and organic chemistry experimentation.