1. Home
  2. 2-pyridin-4-yl-1,3-thiazole-4-carbaldehyde

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

2-pyridin-4-yl-1,3-thiazole-4-carbaldehyde

O=Cc1csc(n1)c1ccncc1 Request for Quotation
Chemical Name: 2-pyridin-4-yl-1,3-thiazole-4-carbaldehyde
CAS Number: 533885-37-9
Product Number: AG00DIVQ(AGN-PC-05C73Y)
Synonyms:
MDL No:
Molecular Formula: C9H6N2OS
Molecular Weight: 190.22174

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-(Pyridin-4-yl)thiazole-4-carbaldehyde is a versatile and crucial compound in chemical synthesis due to its unique structural and reactive properties. This compound is commonly used as a key building block in the synthesis of various organic molecules and pharmaceuticals. Its ability to undergo a variety of reactions, including condensation, nucleophilic addition, and substitution reactions, makes it an essential component in the creation of complex molecular structures. In organic synthesis, 2-(Pyridin-4-yl)thiazole-4-carbaldehyde serves as a valuable intermediate for the preparation of heterocyclic compounds, which are important in medicinal chemistry and the development of bioactive molecules. Additionally, this compound can be utilized in the development of fluorescent probes and dyes, owing to its unique photophysical properties. The application of 2-(Pyridin-4-yl)thiazole-4-carbaldehyde extends to the fields of materials science and chemical biology, showcasing its significance across various disciplines in the realm of chemical synthesis.