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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)-

A 987306

Nc1nc(N2CCNCC2)c2c(n1)C1=C(CC2)O[C@H]2[C@@H]1CCCC2 Request for Quotation
Chemical Name: A 987306
CAS Number: 1082954-71-9
Product Number: AG007UVV(AGN-PC-0OYAC9)
Synonyms:
MDL No:
Molecular Formula: C18H25N5O
Molecular Weight: 327.4240

Identification/Properties

Computed Properties
Molecular Weight:
327.432g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
327.206g/mol
Monoisotopic Mass:
327.206g/mol
Topological Polar Surface Area:
76.3A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
518
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


A 987306 is a versatile compound that plays a crucial role in chemical synthesis processes, particularly in the pharmaceutical and agrochemical industries. With its unique properties, A 987306 serves as a key building block in the creation of various complex molecules. Its reactivity and compatibility with a wide range of functional groups make it an essential component in the synthesis of new drugs, pesticides, and other bioactive compounds. Additionally, A 987306 is known for its high yield and efficiency, making it a preferred choice for chemists seeking to streamline their synthetic routes and optimize their research and development efforts.