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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)-

Thieno[2,3-b]pyridin-6(7H)-one, 4-hydroxy-

O=c1cc(O)c2c([nH]1)scc2 Request for Quotation
Chemical Name: Thieno[2,3-b]pyridin-6(7H)-one, 4-hydroxy-
CAS Number: 99429-78-4
Product Number: AG005SD2(AGN-PC-0AKQ43)
Synonyms:
MDL No:
Molecular Formula: C7H5NO2S
Molecular Weight: 167.1851

Identification/Properties

Properties
BP:
439.7±45.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
167.182g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
167.004g/mol
Monoisotopic Mass:
167.004g/mol
Topological Polar Surface Area:
77.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
227
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


4-Hydroxythieno[2,3-b]pyridin-6(7H)-one serves as a versatile building block in chemical synthesis due to its unique structural features and reactivity. This compound plays a crucial role as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its heterocyclic structure containing a thieno and pyridinone ring provides a diverse range of synthetic possibilities, making it a valuable tool for organic chemists. By exploiting its reactivity, researchers can introduce specific functional groups, modify the aromatic system, and create complex molecular structures in a controlled manner. Additionally, the presence of the hydroxy group offers opportunities for further derivatization, enabling the synthesis of tailored molecules with desired properties for various applications in the fields of medicinal chemistry, materials science, and organic synthesis.