tert-butyl N-[1-(2-chloropyrimidin-4-yl)piperidin-4-yl]carbamate|596817-49-1,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

tert-butyl N-[1-(2-chloropyrimidin-4-yl)piperidin-4-yl]carbamate

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Chemical Name:	tert-butyl N-[1-(2-chloropyrimidin-4-yl)piperidin-4-yl]carbamate
CAS Number:	596817-49-1
Product Number:	AG00IAL7(AGN-PC-08S4PI)
Synonyms:
MDL No:
Molecular Formula:	C14H21ClN4O2
Molecular Weight:	312.7951

Identification/Properties
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NMR Spectrum
Other Analytical Data
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Identification/Properties

Computed Properties

Molecular Weight:

312.798g/mol

XLogP3:

2.9

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

312.135g/mol

Monoisotopic Mass:

312.135g/mol

Topological Polar Surface Area:

67.4A^2

Heavy Atom Count:

Formal Charge:

Complexity:

353

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

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

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Chemical Structure

The tert-Butyl (1-(2-chloropyrimidin-4-yl)piperidin-4-yl)carbamate is a versatile compound commonly utilized in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structure and reactivity.In chemical synthesis, tert-Butyl (1-(2-chloropyrimidin-4-yl)piperidin-4-yl)carbamate can be employed as a key intermediate for the synthesis of complex organic molecules. Its specific functional groups provide sites for further modification, allowing chemists to introduce diverse substituents and tailor the properties of the final product.Additionally, this compound can act as a protecting group in organic synthesis. By strategically incorporating tert-Butyl (1-(2-chloropyrimidin-4-yl)piperidin-4-yl)carbamate into a molecule, certain reactive functional groups can be shielded from unwanted reactions or transformations. This protective role enables selective chemical reactions to occur, facilitating the synthesis of intricate structures with high precision.Overall, the application of tert-Butyl (1-(2-chloropyrimidin-4-yl)piperidin-4-yl)carbamate in chemical synthesis showcases its significance as a pivotal reagent in the construction of complex organic molecules with diverse functionalities and tailored properties.