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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)-

2-Piperidineaceticacid, 1-[(1,1-dimethylethoxy)carbonyl]-, (2R)-

OC(=O)C[C@H]1CCCCN1C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 2-Piperidineaceticacid, 1-[(1,1-dimethylethoxy)carbonyl]-, (2R)-
CAS Number: 351410-32-7
Product Number: AG0032EI(AGN-PC-0O97OT)
Synonyms:
MDL No:
Molecular Formula: C12H21NO4
Molecular Weight: 243.2994

Identification/Properties

Properties
MP:
93-97 °C
BP:
373°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
243.303g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
243.147g/mol
Monoisotopic Mass:
243.147g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
295
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, (R)-1-Boc-2-Piperidineacetic acid is a valuable compound that serves as a versatile building block for the creation of complex organic molecules. This particular compound is commonly used as a chiral auxiliary in asymmetric synthesis, allowing chemists to control the stereochemistry of the reaction products. By utilizing (R)-1-Boc-2-Piperidineacetic acid as a starting material, chemists can introduce chirality into their target molecules with high levels of selectivity and efficiency. Additionally, this compound can also be employed in the synthesis of pharmaceutical intermediates and natural products due to its unique structural features and reactivity. Its strategic incorporation into synthetic routes enables the efficient construction of diverse chemical structures with specific stereochemical properties, making it a valuable tool for synthetic chemists in the design and production of complex molecules.