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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, 2,4-dichloro-

O=Cc1sc(nc1Cl)Cl Request for Quotation
Chemical Name: 5-Thiazolecarboxaldehyde, 2,4-dichloro-
CAS Number: 92972-48-0
Product Number: AG003FQN(AGN-PC-0K5YEV)
Synonyms:
MDL No:
Molecular Formula: C4HCl2NOS
Molecular Weight: 182.0278

Identification/Properties

Properties
MP:
40 °C
BP:
180°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
182.018g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
180.916g/mol
Monoisotopic Mass:
180.916g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
123
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:
Danger
UN#:
2811
Hazard Statements:
H301-H319
Precautionary Statements:
P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dichloro-5-thiazolecarboxaldehyde is a versatile compound widely used in chemical synthesis, particularly in the field of pharmaceuticals and agrochemicals. With its unique structure and reactivity, this compound serves as a key building block in the creation of various important molecules.In organic synthesis, 2,4-Dichloro-5-thiazolecarboxaldehyde is frequently utilized as a starting material for the preparation of thiazole-containing compounds. Its presence can significantly influence the properties and functions of the final products, making it an essential component in the development of novel molecules with diverse applications.Due to its specific chemical properties, 2,4-Dichloro-5-thiazolecarboxaldehyde plays a crucial role in the synthesis of bioactive compounds, pharmaceutical intermediates, and crop protection agents. Its ability to undergo various reactions and transformations allows chemists to access a wide range of molecular structures, enabling the targeted design and synthesis of biologically active molecules with desired properties.Overall, the application of 2,4-Dichloro-5-thiazolecarboxaldehyde in chemical synthesis underscores its importance in modern scientific research and industry, where its role as a valuable building block continues to drive innovation and advancements in pharmaceutical and agricultural chemistry.