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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-chloro-4-cyclopropyl-1,3-thiazole

Clc1scc(n1)C1CC1 Request for Quotation
Chemical Name: 2-chloro-4-cyclopropyl-1,3-thiazole
CAS Number: 1344072-01-0
Product Number: AG007ZZY(AGN-PC-0FFKVP)
Synonyms:
MDL No:
Molecular Formula: C6H6ClNS
Molecular Weight: 159.6365

Identification/Properties

Computed Properties
Molecular Weight:
159.631g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
158.991g/mol
Monoisotopic Mass:
158.991g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
116
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-Chloro-4-cyclopropylthiazole, a versatile chemical compound widely utilized in chemical synthesis, plays a crucial role as a key building block in the creation of pharmaceuticals, agrochemicals, and various functional materials. This compound exhibits remarkable reactivity and selectivity, making it a valuable tool for chemists seeking to introduce specific functionalities into their target molecules. By serving as a pivotal intermediate, 2-Chloro-4-cyclopropylthiazole enables the efficient construction of complex structures through diverse synthetic routes, thereby contributing significantly to the advancement of modern organic chemistry. Its unique properties and compatibility with a broad range of reaction conditions make it an indispensable asset in the realm of chemical synthesis, facilitating the development of novel compounds with diverse applications.