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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)-

2-(2-bromophenyl)-1,3-thiazole-4-carbaldehyde

O=Cc1csc(n1)c1ccccc1Br Request for Quotation
Chemical Name: 2-(2-bromophenyl)-1,3-thiazole-4-carbaldehyde
CAS Number: 885279-14-1
Product Number: AG0089A9(AGN-PC-09OG81)
Synonyms:
MDL No:
Molecular Formula: C10H6BrNOS
Molecular Weight: 268.1297

Identification/Properties

Computed Properties
Molecular Weight:
268.128g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
266.935g/mol
Monoisotopic Mass:
266.935g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
214
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2-Bromophenyl)thiazole-4-carbaldehyde is a versatile compound widely utilized in chemical synthesis, particularly in the field of organic chemistry. Its unique structure and reactivity make it a valuable building block for the creation of various complex molecules and functional materials.In organic synthesis, 2-(2-Bromophenyl)thiazole-4-carbaldehyde serves as a key intermediate in the preparation of diverse chemical entities. Its reactive aldehyde group enables the introduction of various functional groups through selective reactions, allowing chemists to modify its structure to achieve different molecular targets. This compound can participate in a range of transformations, including condensation, reduction, and cross-coupling reactions, making it a valuable tool in the hands of synthetic chemists.Additionally, the thiazole ring in 2-(2-Bromophenyl)thiazole-4-carbaldehyde adds to its utility by providing potential sites for further functionalization. The presence of the bromophenyl substituent further expands its synthetic possibilities, allowing for the introduction of aryl functionalities in the synthesized products.Overall, 2-(2-Bromophenyl)thiazole-4-carbaldehyde plays a crucial role in modern chemical synthesis as a versatile and valuable building block, enabling the efficient construction of complex molecules with diverse applications in pharmaceuticals, materials science, and agrochemicals.