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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)-

tert-butyl 4-(4-cyanophenoxy)piperidine-1-carboxylate

N#Cc1ccc(cc1)OC1CCN(CC1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-(4-cyanophenoxy)piperidine-1-carboxylate
CAS Number: 333954-86-2
Product Number: AG00CKR3(AGN-PC-03XHSC)
Synonyms:
MDL No:
Molecular Formula: C17H22N2O3
Molecular Weight: 302.3682

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
302.374g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
302.163g/mol
Monoisotopic Mass:
302.163g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
419
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
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 tert-Butyl 4-(4-cyanophenoxy)piperidine-1-carboxylate is a versatile compound commonly used in chemical synthesis for its unique properties and diverse applications. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceutical intermediates due to its stable nature and reactivity.In chemical synthesis, tert-Butyl 4-(4-cyanophenoxy)piperidine-1-carboxylate can act as a key starting material in the preparation of complex organic compounds such as drugs, agrochemicals, and functional materials. Its specific structure and functional groups allow for precise manipulation and modification, making it a valuable tool for chemists to design and synthesize novel molecules with specific desired properties.By utilizing tert-Butyl 4-(4-cyanophenoxy)piperidine-1-carboxylate in chemical synthesis, researchers can access a wide range of potential applications in drug discovery, material science, and other fields requiring the development of new molecules with tailored properties. Its compatibility with various reaction conditions and compatibility with different functional groups make it a versatile choice for synthetic chemists seeking to access diverse chemical space and explore new avenues for molecule design and discovery.