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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)-

7H-pyrrolo[2,3-d]pyrimidin-2-amine

Nc1ncc2c(n1)[nH]cc2 Request for Quotation
Chemical Name: 7H-pyrrolo[2,3-d]pyrimidin-2-amine
CAS Number: 93366-88-2
Product Number: AG0063QV(AGN-PC-07AAHG)
Synonyms:
MDL No:
Molecular Formula: C6H6N4
Molecular Weight: 134.1386

Identification/Properties

Properties
BP:
359.786 °C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
134.142g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
134.059g/mol
Monoisotopic Mass:
134.059g/mol
Topological Polar Surface Area:
67.6A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
127
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


7H-Pyrrolo[2,3-d]pyrimidin-2-amine is a versatile and valuable chemical compound frequently utilized in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural features and functional groups. In chemical synthesis, 7H-Pyrrolo[2,3-d]pyrimidin-2-amine acts as a crucial intermediate in the formation of diverse heterocyclic compounds. It participates in various organic reactions, such as nucleophilic substitution, condensation, and cyclization, enabling the generation of complex molecular structures with desired properties and functionalities. Researchers and chemists rely on the strategic incorporation of this compound in synthetic routes to access novel molecules with potential applications in drug discovery, material science, and other fields. Its ability to undergo diverse transformations and form intricate molecular scaffolds make it a valuable tool for the efficient and targeted synthesis of a wide range of compounds with diverse biological and chemical activities.