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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]pyridine, 4,6-dichloro-

Clc1cc(Cl)c2c(n1)scc2 Request for Quotation
Chemical Name: Thieno[2,3-b]pyridine, 4,6-dichloro-
CAS Number: 99429-80-8
Product Number: AG005SD1(AGN-PC-00MQUV)
Synonyms:
MDL No:
Molecular Formula: C7H3Cl2NS
Molecular Weight: 204.0764

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
204.068g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
202.936g/mol
Monoisotopic Mass:
202.936g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,6-Dichlorothieno[2,3-b]pyridine is a versatile building block commonly used in chemical synthesis. This compound is valued for its unique structure and reactivity, making it an essential component in various synthetic pathways. In organic synthesis, 4,6-Dichlorothieno[2,3-b]pyridine serves as a key intermediate in the construction of complex molecules, including pharmaceuticals, agrochemicals, and materials. Its presence in a reaction scheme can facilitate the formation of important functional groups, such as heterocycles, which are prevalent in many biologically active compounds. Furthermore, the substituted thienopyridine core of this molecule offers opportunities for further derivatization, enabling the introduction of specific chemical functionalities to tailor the properties of the final product. This compound's role in chemical synthesis highlights its significance in the development of novel compounds with potential applications across various industries.