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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-Piperidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethyl ester,(2S)-

OCC[C@@H]1CCCCN1C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethyl ester,(2S)-
CAS Number: 199942-74-0
Product Number: AG002CH2(AGN-PC-0QQZWE)
Synonyms:
MDL No:
Molecular Formula: C12H23NO3
Molecular Weight: 229.3159

Identification/Properties

Properties
BP:
324.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
229.32g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
229.168g/mol
Monoisotopic Mass:
229.168g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
235
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:
Danger
UN#:
2810
Hazard Statements:
H301-H320-H400
Precautionary Statements:
P264-P270-P273-P301+P310+P330-P305+P351+P338-P337+P313-P391-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-1-N-Boc-Piperidine-2-ethanol is a versatile chemical compound commonly used in chemical synthesis for its unique properties and reactivity. As a chiral building block, it plays a crucial role in the asymmetric synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. This compound serves as a key intermediate in the preparation of complex molecules by providing a chiral center that imparts stereochemical control in organic reactions. Its Boc (tert-butoxycarbonyl) protecting group helps to prevent unwanted side reactions and allows for selective functional group manipulations during the synthesis process. The piperidine ring confers both structural diversity and biological activity to the molecules synthesized using this compound. Overall, (S)-1-N-Boc-Piperidine-2-ethanol is an indispensable tool for chemists working on the development of new drugs, materials, and other organic compounds.