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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)-

4-cyclopropyl-1,3-thiazole

C1CC1c1ncsc1 Request for Quotation
Chemical Name: 4-cyclopropyl-1,3-thiazole
CAS Number: 433217-34-6
Product Number: AG003LA0(AGN-PC-086DQE)
Synonyms:
MDL No: MFCD07390348
Molecular Formula: C6H7NS
Molecular Weight: 125.1915

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
125.189g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
125.03g/mol
Monoisotopic Mass:
125.03g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
90.5
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-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Cyclopropylthiazole is a valuable building block in chemical synthesis, commonly utilized for its versatile applications in the development of pharmaceuticals, agrochemicals, and materials science. This specialized compound exhibits unique reactivity due to the presence of the cyclopropyl group and the thiazole ring, making it a key component in the synthesis of various organic molecules.One of the primary applications of 4-Cyclopropylthiazole in chemical synthesis is as a precursor for synthesizing heterocyclic compounds. By functionalizing the cyclopropyl group or modifying the thiazole ring, chemists can create a diverse array of complex molecules with potentially valuable properties. Additionally, the presence of the thiazole moiety in 4-Cyclopropylthiazole offers opportunities for selective transformations and the introduction of additional functional groups.Furthermore, 4-Cyclopropylthiazole can serve as a key intermediate in the preparation of biologically active compounds. Its structural features make it a strategic starting material for the synthesis of pharmaceutical agents, herbicides, and other bioactive molecules. Through strategic manipulations of its chemical structure, researchers can explore various pharmacological activities and optimize the properties of the final products.Overall, the versatility and reactivity of 4-Cyclopropylthiazole make it a valuable tool in organic synthesis, enabling chemists to access a wide range of novel compounds with potential applications in diverse fields such as medicine, agriculture, and materials science.