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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)-

Benzaldehyde, 3-(2-thiazolyl)-

O=Cc1cccc(c1)c1nccs1 Request for Quotation
Chemical Name: Benzaldehyde, 3-(2-thiazolyl)-
CAS Number: 885465-97-4
Product Number: AG008BTL(AGN-PC-01XFRF)
Synonyms:
MDL No:
Molecular Formula: C10H7NOS
Molecular Weight: 189.2337

Identification/Properties

Computed Properties
Molecular Weight:
189.232g/mol
XLogP3:
2.1
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:
186
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


3-Thiazol-2-yl-benzaldehyde is a versatile compound that finds extensive application in chemical synthesis. Known for its distinct molecular structure, this compound is valued for its ability to serve as a vital building block in the creation of various organic molecules.In chemical synthesis, 3-Thiazol-2-yl-benzaldehyde plays a crucial role as a key intermediate in the production of a wide range of pharmaceuticals, agrochemicals, and fine chemicals. Its functional groups make it a valuable precursor for the synthesis of more complex molecules with diverse applications. This compound's unique characteristics enable chemists to introduce specific functionalities and modify molecular structures to achieve desired properties in the final product.Furthermore, 3-Thiazol-2-yl-benzaldehyde is utilized in the development of novel materials and as a key component in the creation of catalysts and ligands for various chemical reactions. Its reactivity and compatibility with different synthetic pathways make it a sought-after ingredient in the field of organic chemistry.Overall, the application of 3-Thiazol-2-yl-benzaldehyde in chemical synthesis underscores its importance as a fundamental building block that enables the creation of innovative compounds with specialized functions and properties.