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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)-

Thiazole, 2-chloro-4-ethyl-

CCc1csc(n1)Cl Request for Quotation
Chemical Name: Thiazole, 2-chloro-4-ethyl-
CAS Number: 98025-12-8
Product Number: AG00H6ML(AGN-PC-0NHS1X)
Synonyms:
MDL No:
Molecular Formula: C5H6ClNS
Molecular Weight: 147.6258

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
147.62g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
146.991g/mol
Monoisotopic Mass:
146.991g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
78.8
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#:
-
Hazard Statements:
H302-H312-H315-H319-H332-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-4-ethylthiazole is a versatile chemical compound commonly utilized in chemical synthesis processes. This compound plays a crucial role as a building block in the creation of various organic molecules with unique functionalities and properties. Due to its specific structure and reactivity, 2-Chloro-4-ethylthiazole is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its incorporation in the synthesis of complex molecules allows for the introduction of specific functionalities and enhances the overall efficiency of the synthetic pathways. Additionally, the presence of the chlorine and ethyl groups in the thiazole ring provides opportunities for further modification and diversification, making it a valuable tool for chemists and researchers in a wide range of industries.