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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)-

3-phenyl-2-propylsulfanyl-6,7-dihydrothieno[3,2-d]pyrimidin-4-one

CCCSc1nc2CCSc2c(=O)n1c1ccccc1 Request for Quotation
Chemical Name: 3-phenyl-2-propylsulfanyl-6,7-dihydrothieno[3,2-d]pyrimidin-4-one
CAS Number: 686770-80-9
Product Number: AG00FHTU(AGN-PC-0KBL9A)
Synonyms:
MDL No: MFCD04457614
Molecular Formula: C15H16N2OS2
Molecular Weight: 304.4303

Identification/Properties

Computed Properties
Molecular Weight:
304.426g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
304.07g/mol
Monoisotopic Mass:
304.07g/mol
Topological Polar Surface Area:
83.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
453
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


BC 11-38, also known as 1-benzyl-1H-1,2,3-triazole-4-carboxamide, is a versatile molecule widely employed in the field of chemical synthesis. With its unique structure and reactivity, BC 11-38 serves as a valuable building block in the creation of various complex organic compounds. Its role in chemical synthesis encompasses several key applications, including:1. Click Chemistry: BC 11-38 is commonly utilized in click reactions, a powerful approach in organic chemistry for the facile assembly of molecules. By participating in azide-alkyne cycloaddition reactions, BC 11-38 can link different functional groups together to form diverse products efficiently.2. Medicinal Chemistry: The presence of a triazole moiety in BC 11-38 makes it an attractive candidate for drug discovery and development. This compound can be functionalized further to incorporate pharmacophores, enhancing its biological activity and properties as a potential drug candidate.3. Ligand Synthesis: BC 11-38 can be modified to serve as a ligand in coordination complexes for catalysis or material applications. Its ability to chelate metal ions and participate in coordination chemistry offers a versatile platform for designing new catalysts or functional materials.4. Peptide Chemistry: BC 11-38 can be integrated into peptide structures to confer stability and resistance to enzymatic degradation. By introducing this moiety at specific positions within a peptide sequence, researchers can modulate the peptide's properties for various biological or therapeutic applications.Overall, BC 11-38's unique chemical structure and versatile reactivity make it a valuable asset in chemical synthesis, enabling the creation of diverse compounds with tailored properties for pharmaceutical, material science, and catalysis research.