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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)-

7-chloro-3-methylthieno[3,2-b]pyridine

Cc1csc2c1nccc2Cl Request for Quotation
Chemical Name: 7-chloro-3-methylthieno[3,2-b]pyridine
CAS Number: 953045-91-5
Product Number: AG0039LG(AGN-PC-0BSYUY)
Synonyms:
MDL No:
Molecular Formula: C8H6ClNS
Molecular Weight: 183.6579

Identification/Properties

Computed Properties
Molecular Weight:
183.653g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
182.991g/mol
Monoisotopic Mass:
182.991g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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


7-Chloro-3-methylthieno[3,2-b]pyridine is a versatile building block in organic chemical synthesis. It is commonly used as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique structure and reactivity, 7-Chloro-3-methylthieno[3,2-b]pyridine plays a crucial role in the synthesis of biologically active compounds and functional materials. Its substituted pyridine ring enables the introduction of various functional groups, allowing for the creation of diverse chemical structures with specific properties and activities. This compound is particularly valued for its role in creating new molecules with potential applications in drug discovery, materials science, and chemical research.