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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)-

methyl 4-chlorothieno[2,3-c]pyridine-2-carboxylate

COC(=O)c1sc2c(c1)c(Cl)cnc2 Request for Quotation
Chemical Name: methyl 4-chlorothieno[2,3-c]pyridine-2-carboxylate
CAS Number: 251996-85-7
Product Number: AG002QUR(AGN-PC-01XAT1)
Synonyms:
MDL No:
Molecular Formula: C9H6ClNO2S
Molecular Weight: 227.6674

Identification/Properties

Computed Properties
Molecular Weight:
227.662g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
226.981g/mol
Monoisotopic Mass:
226.981g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
239
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


Methyl 4-chlorothieno[2,3-c]pyridine-2-carboxylate is a versatile compound widely used in chemical synthesis due to its unique structural properties. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and organic materials. Its substituted thieno[2,3-c]pyridine core provides opportunities for the synthesis of heterocyclic compounds with diverse functionalities, making it an essential component in drug discovery and development. Additionally, the presence of the ester group in this molecule facilitates further derivatization, allowing for the generation of structurally diverse analogs for biological screening and structure-activity relationship studies. In summary, Methyl 4-chlorothieno[2,3-c]pyridine-2-carboxylate is a valuable tool in the hands of synthetic chemists for the construction of complex molecules with potential applications in various industries.