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Home  > 7-(Chloromethyl)-3-methyl-5h-[1,3]thiazolo[3,2-a]pyrimidin-5-one

AE48890

100003-81-4 | 7-(Chloromethyl)-3-methyl-5h-[1,3]thiazolo[3,2-a]pyrimidin-5-one

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% 1 week $446.00 $312.00 -   +
500mg 95% 1 week $656.00 $459.00 -   +
1g 95% 1 week $820.00 $574.00 -   +
2.5g 95% 1 week $1,330.00 $931.00 -   +
5g 95% 1 week $2,181.00 $1,527.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE48890
Chemical Name: 7-(Chloromethyl)-3-methyl-5h-[1,3]thiazolo[3,2-a]pyrimidin-5-one
CAS Number: 100003-81-4
Molecular Formula: C8H7ClN2OS
Molecular Weight: 214.672
MDL Number: MFCD06655025
SMILES: ClCc1cc(=O)n2c(n1)scc2C

 

Upstream Synthesis Route
  • The compound 7-(Chloromethyl)-3-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one is a valuable reagent in chemical synthesis due to its versatile properties. With its unique structure and functional groups, this compound serves as a key building block in the preparation of various biologically active molecules and pharmaceutical intermediates. In organic synthesis, 7-(Chloromethyl)-3-methyl-5H-thiazolo[3,2-a]pyrimidin-5-one can act as a precursor for the introduction of a chloromethyl group into a target molecule. The chloromethyl group can undergo further reactions such as nucleophilic substitution, Suzuki coupling, or palladium-catalyzed cross-coupling reactions to generate diverse chemical entities. Furthermore, the thiazolo[3,2-a]pyrimidine moiety in this compound can participate in various synthetic transformations, allowing for the preparation of heterocyclic compounds with potential biological activities. By strategically incorporating this building block into synthetic pathways, chemists can access a wide range of novel compounds for drug discovery and materials science applications.
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