1. Home
  2. 5-Thiazolecarboxylic acid, 2-bromo-4-methyl-, ethyl ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

5-Thiazolecarboxylic acid, 2-bromo-4-methyl-, ethyl ester

Cc1nc(sc1C(=O)OCC)Br Request for Quotation
Chemical Name: 5-Thiazolecarboxylic acid, 2-bromo-4-methyl-, ethyl ester
CAS Number: 22900-83-0
Product Number: AG002LE9(AGN-PC-0KLR3H)
Synonyms:
MDL No: MFCD03791227
Molecular Formula: C7H8BrNO2S
Molecular Weight: 250.1129

Identification/Properties

Properties
MP:
70 - 71 °C
BP:
287°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
250.11g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
248.946g/mol
Monoisotopic Mass:
248.946g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
179
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

Request for Quotation

Customer Feedback

Chemical Structure


The application of Ethyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylate in chemical synthesis lies in its versatile reactivity and functional group interconversion capabilities. This compound serves as a crucial building block in the synthesis of various pharmaceutically active molecules and agrochemicals due to its ability to participate in a wide range of synthetic transformations.Ethyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylate can undergo substitution reactions to introduce different functional groups at the 2-position of the thiazole ring, thereby enabling the synthesis of diverse thiazole derivatives with tailored properties. Furthermore, the carboxylate moiety in this compound serves as a handle for further derivatization, allowing for the attachment of other molecular fragments to create more complex structures.Overall, Ethyl 2-bromo-4-methyl-1,3-thiazole-5-carboxylate plays a crucial role in chemical synthesis by serving as a key intermediate for the construction of biologically active compounds and advanced materials through strategic functionalization and modification pathways.