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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-(chloromethyl)-5-methyl-1,3-thiazole

Cc1cnc(s1)CCl Request for Quotation
Chemical Name: 2-(chloromethyl)-5-methyl-1,3-thiazole
CAS Number: 921145-23-5
Product Number: AG00IH0W(AGN-PC-02VEQP)
Synonyms:
MDL No:
Molecular Formula: C5H6ClNS
Molecular Weight: 147.6258

Identification/Properties

Computed Properties
Molecular Weight:
147.62g/mol
XLogP3:
1.8
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Chloromethyl)-5-methylthiazole is a versatile compound widely used in organic synthesis for various chemical applications. Its unique structure and reactivity make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. In chemical synthesis, this compound serves as a key intermediate in the preparation of complex molecules by participating in a range of reactions such as nucleophilic substitutions, condensations, and cyclization reactions. Its chloromethyl group enables selective functionalization and manipulation of its molecular structure, allowing for the synthesis of diverse compounds with tailored properties and functionalities. Additionally, the presence of the thiazole ring imparts specific aromatic and heterocyclic characteristics to the molecules, making them of interest in medicinal chemistry and material science. Overall, 2-(Chloromethyl)-5-methylthiazole plays a crucial role in the efficient and strategic construction of intricate organic molecules for various industrial applications.