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Brc1cnc(nc1)C
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)-

methyl 1-(6-chloropyrimidin-4-yl)piperidine-4-carboxylate

COC(=O)C1CCN(CC1)c1ncnc(c1)Cl Request for Quotation
Chemical Name: methyl 1-(6-chloropyrimidin-4-yl)piperidine-4-carboxylate
CAS Number: 914347-88-9
Product Number: AG006MQF(AGN-PC-03NS2Q)
Synonyms:
MDL No:
Molecular Formula: C11H14ClN3O2
Molecular Weight: 255.7008

Identification/Properties

Properties
BP:
395.6°C at 760 mmHg
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The product $name$ plays a crucial role in chemical synthesis as it serves as a key building block for the formation of various organic compounds. Specifically, Methyl 1-(6-chloropyrimidin-4-yl)piperidine-4-carboxylate is commonly utilized in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique molecular structure allows for versatile reactivity, enabling it to participate in a wide range of chemical transformations such as cross-coupling reactions, nucleophilic substitutions, and heterocycle synthesis. By incorporating this compound into synthetic pathways, chemists can access a diverse array of complex molecules with valuable properties and applications.