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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)-

5-Thiazolecarboxaldehyde, 2-chloro-

Clc1ncc(s1)C=O Request for Quotation
Chemical Name: 5-Thiazolecarboxaldehyde, 2-chloro-
CAS Number: 95453-58-0
Product Number: AG00339S(AGN-PC-0K5T3B)
Synonyms:
MDL No: MFCD01568717
Molecular Formula: C4H2ClNOS
Molecular Weight: 147.5828

Identification/Properties

Properties
MP:
85-88°C
BP:
278.6°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Stability:
Air Sensitive
Computed Properties
Molecular Weight:
147.576g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
146.955g/mol
Monoisotopic Mass:
146.955g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
100
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

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Chemical Structure


2-Chloro-1,3-thiazole-5-carboxaldehyde is a versatile chemical compound widely used in chemical synthesis for its unique reactivity and functional groups. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-Chloro-1,3-thiazole-5-carboxaldehyde can be used as a precursor in the production of heterocyclic compounds. Its thiazole ring structure and aldehyde group provide opportunities for structural modifications, making it a valuable intermediate for the synthesis of diverse molecules. This compound is particularly important in the development of new drugs and biologically active compounds due to its ability to easily undergo derivatization reactions.Furthermore, the presence of a chloro group enhances the reactivity of 2-Chloro-1,3-thiazole-5-carboxaldehyde, allowing for selective transformations and functionalization. This reagent can participate in a variety of synthetic pathways, such as condensation, cyclization, and substitution reactions, leading to the formation of complex molecular frameworks with tailored properties.Overall, the strategic application of 2-Chloro-1,3-thiazole-5-carboxaldehyde in chemical synthesis enables the efficient construction of novel compounds with potential applications in pharmaceutical, agricultural, and material science industries.