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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-Piperidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-

OC(=O)CC1CCCCN1C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 2-Piperidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-
CAS Number: 149518-50-3
Product Number: AG001LS4(AGN-PC-0K6A3U)
Synonyms:
MDL No: MFCD02179000
Molecular Formula: C12H21NO4
Molecular Weight: 243.2994

Identification/Properties

Properties
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:
0
Undefined Atom Stereocenter Count:
1
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


1-Boc-2-Piperidineacetic acid, also known as tert-butyloxycarbonyl-2-piperidineacetic acid, is a versatile compound widely used in chemical synthesis due to its unique properties. This compound serves as a crucial building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. One of its primary applications is as a protecting group in organic synthesis, specifically in the protection of amines.By using 1-Boc-2-Piperidineacetic acid as a protecting group, chemists can temporarily shield the amine functional group from unwanted reactions during the synthesis process. This protection allows for selective reactions at other sites on the molecule, enabling the synthesis of complex organic compounds with precision and efficiency. Once the desired reactions are complete, the Boc group can be easily removed under mild conditions, revealing the free amine group in the final product.Furthermore, 1-Boc-2-Piperidineacetic acid's stability and compatibility with a wide range of reaction conditions make it an indispensable tool in the synthesis of peptides, natural products, and other bioactive molecules. Its ease of handling and reliability in chemical transformations have cemented its place as a valuable reagent in the toolkit of synthetic chemists across various industries.