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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)-

Methanone, 2-pyridinyl-2-thienyl-

O=C(c1cccs1)c1ccccn1 Request for Quotation
Chemical Name: Methanone, 2-pyridinyl-2-thienyl-
CAS Number: 6602-63-7
Product Number: AG00FAQH(AGN-PC-0BSASL)
Synonyms:
MDL No:
Molecular Formula: C10H7NOS
Molecular Weight: 189.2337

Identification/Properties

Properties
BP:
333.3°C at 760 mmHg
Computed Properties
Molecular Weight:
189.232g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
189.025g/mol
Monoisotopic Mass:
189.025g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
195
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#:
N/A
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Pyridin-2-yl(thiophen-2-yl)methanone is highly valued in chemical synthesis for its versatile application as a key building block in the creation of various organic compounds. This compound serves as a crucial intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals due to its ability to participate in a wide range of chemical reactions.In organic synthesis, Pyridin-2-yl(thiophen-2-yl)methanone is commonly used for the construction of heterocyclic structures, which are prevalent in biologically active compounds. Its unique structure provides opportunities for functional group manipulations, enabling chemists to introduce diverse functionalities into the target molecules. This compound can undergo reactions such as nucleophilic addition, acylation, and cross-coupling reactions to yield complex molecules with tailored properties.Furthermore, Pyridin-2-yl(thiophen-2-yl)methanone plays a significant role in the development of new materials by serving as a precursor for the synthesis of polymers, dendrimers, and other advanced materials. Its compatibility with various polymerization techniques allows for the incorporation of this building block into polymer chains, leading to materials with specific functionalities and desired characteristics.Overall, the versatile nature of Pyridin-2-yl(thiophen-2-yl)methanone makes it a valuable tool in chemical synthesis, offering endless possibilities for the creation of diverse organic compounds with applications in pharmaceuticals, agrochemicals, materials science, and beyond.