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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)-

Carbamic acid, [2-(4-pyridinyloxy)ethyl]-, 1,1-dimethylethyl ester

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Chemical Name: Carbamic acid, [2-(4-pyridinyloxy)ethyl]-, 1,1-dimethylethyl ester
CAS Number: 379264-77-4
Product Number: AG01JIL0(AGN-PC-0NHWA0)
Synonyms:
MDL No:
Molecular Formula: C12H18N2O3
Molecular Weight: 238.28292

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Chemical Structure


The tert-Butyl (2-(pyridin-4-yloxy)ethyl)carbamate is a versatile compound widely used in chemical synthesis for its unique properties and functionality. This compound is a valuable building block in organic chemistry, particularly in the field of medicinal chemistry and drug development. In chemical synthesis, tert-Butyl (2-(pyridin-4-yloxy)ethyl)carbamate serves as a key intermediate for the preparation of various biologically active molecules and pharmaceutical compounds. Its reactive groups allow for easy manipulation and functionalization, enabling chemists to introduce specific functional groups or structural motifs during the synthesis of complex molecules.One of the key applications of tert-Butyl (2-(pyridin-4-yloxy)ethyl)carbamate is in the modification of natural products or bioactive compounds to enhance their pharmacological properties or develop structure-activity relationships. By incorporating this compound into the molecular structure, chemists can modify the physicochemical properties of the target molecule, such as solubility, stability, or bioavailability.Furthermore, tert-Butyl (2-(pyridin-4-yloxy)ethyl)carbamate can also be used as a protecting group for sensitive functional groups during multi-step synthesis. This compound acts as a temporary shield, preventing undesired reactions and protecting specific sites on the molecule until the desired transformation is complete. Once the desired reactions have been carried out, the protecting group can be easily removed under mild conditions to reveal the reactive functional groups.Overall, the application of tert-Butyl (2-(pyridin-4-yloxy)ethyl)carbamate in chemical synthesis offers chemists a powerful tool to design and construct complex molecules with precision and efficiency. Its versatility and compatibility with various synthetic methods make it a valuable asset in the development of novel pharmaceuticals, agrochemicals, and materials with tailored properties.