tert-butyl 4-(5-formyl-4-methyl-1,3-thiazol-2-yl)piperidine-1-carboxylate


Chemical Name: tert-butyl 4-(5-formyl-4-methyl-1,3-thiazol-2-yl)piperidine-1-carboxylate
CAS Number: 850374-97-9
Product Number: AG004SVE(AGN-PC-0LK8FA)
Synonyms:
MDL No:
Molecular Formula: C15H22N2O3S
Molecular Weight: 310.4118

Identification/Properties


Properties
MP:
220 °C
BP:
440.158 °C at 760 mmHg
Form:
Solid
Computed Properties
Molecular Weight:
310.412g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
310.135g/mol
Monoisotopic Mass:
310.135g/mol
Topological Polar Surface Area:
87.7A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
389
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


Request for Quotation


Customer Feedback


Chemical Structure



The versatile compound 1,1-Dimethylethyl 4-(5-formyl-4-methyl-2-thiazolyl)-1-piperidinecarboxylate plays a pivotal role in chemical synthesis processes. This compound is commonly utilized as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its unique structural features and reactivity. In chemical synthesis, it serves as a crucial building block for creating complex organic molecules with specific biological activities. By incorporating this compound into synthetic routes, chemists can access a diverse range of potential products with tailored properties and functionalities. Its strategic placement within synthetic pathways enables efficient and controlled transformations, facilitating the synthesis of novel compounds for various industrial applications.