1. Home
  2. methyl 2-(4-bromophenyl)-1,3-thiazole-4-carboxylate

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)-

methyl 2-(4-bromophenyl)-1,3-thiazole-4-carboxylate

COC(=O)c1csc(n1)c1ccc(cc1)Br Request for Quotation
Chemical Name: methyl 2-(4-bromophenyl)-1,3-thiazole-4-carboxylate
CAS Number: 1208081-39-3
Product Number: AG00924P(AGN-PC-0BSGRR)
Synonyms:
MDL No:
Molecular Formula: C11H8BrNO2S
Molecular Weight: 298.1557

Identification/Properties

Computed Properties
Molecular Weight:
298.154g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
296.946g/mol
Monoisotopic Mass:
296.946g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
256
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Methyl 2-(4-bromophenyl)thiazole-4-carboxylate is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound plays a crucial role in the construction of complex molecules, particularly in the pharmaceutical and agrochemical industries. Its functional groups make it an ideal building block for the synthesis of various organic compounds through various synthetic strategies.In organic synthesis, Methyl 2-(4-bromophenyl)thiazole-4-carboxylate serves as a key intermediate for the preparation of diverse heterocyclic compounds. Its thiazole ring backbone provides a solid foundation for structural modifications, allowing chemists to introduce additional functionalities and tailor the compound's properties for specific applications. Furthermore, the presence of the ester group enhances the compound's reactivity, enabling selective functionalization and cross-coupling reactions with other organic substrates.Moreover, the bromine atom attached to the phenyl ring offers a reactive site for further derivatization, enabling the synthesis of diverse chemical entities with varied biological activities. By utilizing Methyl 2-(4-bromophenyl)thiazole-4-carboxylate as a key building block, chemists can access a wide range of potential drug candidates, agrochemicals, and materials with tailored properties and functions. This compound's versatility and synthetic utility make it a valuable tool in modern organic synthesis, driving innovation and discovery in the field of chemistry.