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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]pyridine-2-carboxaldehyde

O=Cc1cc2c(s1)ccnc2 Request for Quotation
Chemical Name: Thieno[3,2-c]pyridine-2-carboxaldehyde
CAS Number: 94226-19-4
Product Number: AG006O9K(AGN-PC-02TMBK)
Synonyms:
MDL No:
Molecular Formula: C8H5NOS
Molecular Weight: 163.1964

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
163.194g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
163.009g/mol
Monoisotopic Mass:
163.009g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
162
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Thieno[3,2-c]pyridine-2-carbaldehyde is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various organic compounds. Its unique structure and reactivity make it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and materials. In organic chemistry, Thieno[3,2-c]pyridine-2-carbaldehyde serves as a precursor for the synthesis of heterocyclic compounds with potential biological activities. Furthermore, its functional group can undergo various chemical transformations, including condensation reactions, nucleophilic additions, and cross-coupling reactions, enabling the efficient assembly of complex molecular structures. As a result, this compound plays a crucial role in the development of novel molecules with diverse applications in medicinal chemistry and material science.