5-Thiazolecarboxaldehyde, 2,4-dimethyl-


Chemical Name: 5-Thiazolecarboxaldehyde, 2,4-dimethyl-
CAS Number: 95453-54-6
Product Number: AG003FUR(AGN-PC-0KKXE7)
Synonyms:
MDL No:
Molecular Formula: C6H7NOS
Molecular Weight: 141.1909

Identification/Properties


Properties
MP:
23-27 °C(lit.)
BP:
238.884 °C at 760 mmHg
Storage:
2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
141.188g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
141.025g/mol
Monoisotopic Mass:
141.025g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
118
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-H312-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-Thiazolecarboxaldehyde, 2,4-dimethyl-, is a versatile chemical compound widely utilized in chemical synthesis for its unique properties and applications. This aldehyde derivative serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals due to its ability to participate in a range of chemical reactions.One of the primary applications of 5-Thiazolecarboxaldehyde, 2,4-dimethyl-, is as a key intermediate in the synthesis of heterocyclic compounds. Its thiazole ring structure provides a reactive site for functionalization, allowing for the introduction of diverse chemical groups and modifications. This versatility makes it an essential component in the preparation of bioactive molecules and complex organic compounds.In organic synthesis, this compound acts as a valuable starting material for the construction of thiazole-based derivatives with diverse pharmacological activities. By employing various synthetic strategies such as condensation reactions, C-H functionalization, and cross-coupling reactions, chemists can access a wide range of structurally diverse compounds with potential therapeutic applications.Furthermore, 5-Thiazolecarboxaldehyde, 2,4-dimethyl-, plays a crucial role in the development of novel catalysts and ligands for asymmetric synthesis. Its functional groups can be selectively modified to tailor the reactivity and selectivity of the resulting catalyst, enabling the efficient synthesis of chiral compounds and enantiomerically pure products.Overall, the use of 5-Thiazolecarboxaldehyde, 2,4-dimethyl-, in chemical synthesis showcases its significance as a versatile building block with broad applications in the creation of complex organic molecules and functional materials. Its specific chemical properties and reactivity make it a valuable tool for researchers and chemists working in various fields of chemical science.