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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)-

2,4,7-Pteridinetriamine, 6-phenyl-

Nc1nc(N)c2c(n1)nc(c(n2)c1ccccc1)N Request for Quotation
Chemical Name: 2,4,7-Pteridinetriamine, 6-phenyl-
CAS Number: 396-01-0
Product Number: AG003FOL(AGN-PC-07A27M)
Synonyms:
MDL No:
Molecular Formula: C12H11N7
Molecular Weight: 253.2626

Identification/Properties

Properties
MP:
316°C
BP:
386.46°C (rough estimate)
Storage:
2-8℃;
Form:
Solid
Refractive Index:
1.8260 (estimate)
Solubility:
formic acid: soluble200 mg + 4 mL warm Formic Acid, clear, yellow-green
Computed Properties
Molecular Weight:
253.269g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
1
Exact Mass:
253.108g/mol
Monoisotopic Mass:
253.108g/mol
Topological Polar Surface Area:
130A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
307
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


2,4,7-Triamino-6-phenylpteridine is a versatile compound that finds essential application in chemical synthesis. This unique molecule is utilized as a key building block in the creation of various organic compounds due to its distinct chemical properties. In chemical synthesis, 2,4,7-Triamino-6-phenylpteridine serves as a valuable intermediate for the production of complex molecules with specific structures and functions. Its reactivity and stability make it an ideal starting material for the construction of various pharmaceuticals, agrochemicals, and specialty chemicals. By incorporating 2,4,7-Triamino-6-phenylpteridine into synthetic pathways, chemists can efficiently access a diverse array of target compounds with tailored properties and applications.