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

O=Cc1csc(n1)c1cccc(c1)Br Request for Quotation
Chemical Name: 2-(3-bromophenyl)-1,3-thiazole-4-carbaldehyde
CAS Number: 750624-69-2
Product Number: AG008O4P(AGN-PC-0KCEHB)
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


The 2-(3-Bromophenyl)thiazole-4-carbaldehyde plays a crucial role in chemical synthesis as a versatile building block. It serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. This compound's unique structure and reactive properties make it an essential component in the production of various organic molecules with valuable biological or industrial applications.In chemical synthesis, 2-(3-Bromophenyl)thiazole-4-carbaldehyde can undergo various reactions such as nucleophilic addition, cross-coupling, condensation, and reduction, enabling the formation of complex molecular structures. Its presence in the synthesis pathway can introduce specific functionalities or structural motifs that are important for achieving the desired properties in the final product.Due to its versatility and compatibility with a wide range of synthetic strategies, 2-(3-Bromophenyl)thiazole-4-carbaldehyde is widely employed by chemists in the preparation of diverse compounds with targeted properties. Whether it is used as a starting material, a key intermediate, or a functional group modifier, this compound significantly contributes to the advancement of chemical synthesis in various fields.