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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)-

5-bromo-3H-thieno[2,3-d]pyrimidin-4-one

Brc1csc2c1c(=O)nc[nH]2 Request for Quotation
Chemical Name: 5-bromo-3H-thieno[2,3-d]pyrimidin-4-one
CAS Number: 1239460-83-3
Product Number: AG000L97(AGN-PC-0D1BX6)
Synonyms:
MDL No:
Molecular Formula: C6H3BrN2OS
Molecular Weight: 231.0698

Identification/Properties

Computed Properties
Molecular Weight:
231.067g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
229.915g/mol
Monoisotopic Mass:
229.915g/mol
Topological Polar Surface Area:
69.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
221
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromothieno[2,3-d]pyrimidin-4(1H)-one is a versatile chemical compound widely utilized in chemical synthesis. With its unique structure and reactivity, this compound serves as a valuable building block in various organic reactions.One of the key applications of 5-Bromothieno[2,3-d]pyrimidin-4(1H)-one in chemical synthesis is its role as a precursor for the synthesis of medicinally important heterocyclic compounds. By incorporating this compound into different synthetic pathways, researchers can access structurally diverse molecules with potential pharmaceutical activities.Furthermore, 5-Bromothieno[2,3-d]pyrimidin-4(1H)-one can participate in cross-coupling reactions, nucleophilic substitutions, and cyclization reactions, allowing for the construction of complex molecular frameworks. Its ability to undergo various transformations makes it a valuable tool for chemists seeking to create new compounds with tailored properties.Overall, 5-Bromothieno[2,3-d]pyrimidin-4(1H)-one plays a crucial role in modern chemical synthesis by enabling the efficient and selective formation of intricate organic molecules with diverse applications.