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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)-

[1,3]Oxathiolo[5,4-c]pyridine-6-carboxaldehyde

O=Cc1ncc2c(c1)SCO2 Request for Quotation
Chemical Name: [1,3]Oxathiolo[5,4-c]pyridine-6-carboxaldehyde
CAS Number: 872714-69-7
Product Number: AG008EJV(AGN-PC-0CV8S6)
Synonyms:
MDL No:
Molecular Formula: C7H5NO2S
Molecular Weight: 167.1851

Identification/Properties

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


[1,3]Oxathiolo[5,4-c]pyridine-6-carbaldehyde is a versatile compound that finds extensive application in chemical synthesis as a key intermediate in the preparation of various functional materials. This compound serves as a valuable building block for the construction of a wide range of heterocyclic compounds due to its unique structural features and reactivity. In organic synthesis, [1,3]Oxathiolo[5,4-c]pyridine-6-carbaldehyde is utilized as a precursor for the synthesis of complex molecules with diverse pharmacological and material properties. Its ability to undergo various transformations, including substitution, oxidation, and reduction reactions, makes it a valuable tool for the creation of novel compounds with tailored functionalities. Additionally, [1,3]Oxathiolo[5,4-c]pyridine-6-carbaldehyde has been employed in the development of new synthetic methodologies and strategies for the production of high-value chemical entities. Its versatile nature and compatibility with different reaction conditions make it an indispensable component in the toolbox of synthetic chemists striving to access structurally diverse and biologically active molecules.