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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)-

(S)-3-CARBOXYMETHYL-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

OC(=O)C[C@@H]1CCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: (S)-3-CARBOXYMETHYL-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
CAS Number: 941289-27-6
Product Number: AG00GRWC(AGN-PC-0ONTGO)
Synonyms:
MDL No:
Molecular Formula: C12H21NO4
Molecular Weight: 243.2994

Identification/Properties

Computed Properties
Molecular Weight:
243.303g/mol
XLogP3:
1.4
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2-(1-(tert-Butoxycarbonyl)piperidin-3-yl)acetic acid is a versatile compound widely utilized in chemical synthesis as a chiral building block. This compound plays a crucial role in asymmetric synthesis due to its configuration and functional groups, allowing for the creation of complex molecules with high stereochemical purity. In particular, it is commonly employed in the construction of pharmaceutical intermediates and natural product synthesis. Its unique structural features and chirality make it a valuable tool for the development of new synthetic routes and the preparation of enantioenriched compounds in a controlled manner.