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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[3,2-c]pyridin-4(5H)-one

O=c1[nH]ccc2c1ccs2 Request for Quotation
Chemical Name: Thieno[3,2-c]pyridin-4(5H)-one
CAS Number: 27685-92-3
Product Number: AG002UFT(AGN-PC-0JPA63)
Synonyms:
MDL No:
Molecular Formula: C7H5NOS
Molecular Weight: 151.1857

Identification/Properties

Properties
BP:
406.041°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
151.183g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
151.009g/mol
Monoisotopic Mass:
151.009g/mol
Topological Polar Surface Area:
57.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
190
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Thieno[3,2-c]pyridin-4-ol, a versatile heterocyclic compound, finds wide application in chemical synthesis as a valuable building block in organic chemistry. This unique molecule serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. With its distinct structural features, Thieno[3,2-c]pyridin-4-ol enables the construction of complex molecules through diverse chemical transformations, such as oxidation, reduction, and functional group interconversions. In particular, its aromatic ring system and hydroxyl group offer opportunities for selective derivatization, facilitating the preparation of structurally diverse compounds for biological testing and material science research. Furthermore, the presence of nitrogen and sulfur atoms in the heterocyclic skeleton imparts special reactivity characteristics, making Thieno[3,2-c]pyridin-4-ol a valuable tool for synthetic chemists seeking to modulate the properties and functions of organic compounds.