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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)-

1-Piperidinyloxy, 4-amino-4-carboxy-2,2,6,6-tetramethyl-

OC(=O)C1(N)CC(C)(C)N(C(C1)(C)C)[O] Request for Quotation
Chemical Name: 1-Piperidinyloxy, 4-amino-4-carboxy-2,2,6,6-tetramethyl-
CAS Number: 15871-57-5
Product Number: AG001QS8(AGN-PC-0Q7JIO)
Synonyms:
MDL No:
Molecular Formula: C10H19N2O3
Molecular Weight: 215.2695

Identification/Properties

Computed Properties
Molecular Weight:
215.273g/mol
XLogP3:
-2.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
215.14g/mol
Monoisotopic Mass:
215.14g/mol
Topological Polar Surface Area:
67.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
268
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Piperidinyloxy, 4-amino-4-carboxy-2,2,6,6-tetramethyl- is a versatile compound widely used in chemical synthesis. Its unique structure containing a piperidinyloxy moiety makes it valuable for various applications in organic chemistry.This compound is commonly employed as a radical initiator in polymerization reactions, particularly in the synthesis of novel polymers with tailored properties. Its stable free radical nature allows for controlled initiation of polymer chains, leading to enhanced control over polymer molecular weight and dispersity.Additionally, 1-Piperidinyloxy, 4-amino-4-carboxy-2,2,6,6-tetramethyl- can act as a radical scavenger in oxidative transformations, playing a key role in inhibiting unwanted side reactions and promoting selective bond formation. This feature makes it a valuable tool in the development of efficient synthetic pathways for the production of complex organic molecules.Furthermore, this compound can also function as a catalyst in certain oxidation reactions, facilitating the conversion of substrates to desired products through mild and sustainable reaction conditions. Its ability to promote specific bond cleavage and formation makes it a valuable asset in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.In summary, 1-Piperidinyloxy, 4-amino-4-carboxy-2,2,6,6-tetramethyl- is a versatile reagent with diverse applications in chemical synthesis, offering unique opportunities for the design and execution of advanced synthetic strategies.