1. Home
  2. 1,3-Piperidinedicarboxylicacid, 1-(1,1-dimethylethyl) ester, 3-hydrazide, (3S)-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

1,3-Piperidinedicarboxylicacid, 1-(1,1-dimethylethyl) ester, 3-hydrazide, (3S)-

NNC(=O)[C@H]1CCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1,3-Piperidinedicarboxylicacid, 1-(1,1-dimethylethyl) ester, 3-hydrazide, (3S)-
CAS Number: 625470-88-4
Product Number: AG00E99G(AGN-PC-0T4YJE)
Synonyms:
MDL No:
Molecular Formula: C11H21N3O3
Molecular Weight: 243.3027

Identification/Properties

Computed Properties
Molecular Weight:
243.307g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
243.158g/mol
Monoisotopic Mass:
243.158g/mol
Topological Polar Surface Area:
84.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
299
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The (S)-tert-Butyl 1-(piperidine-3-carbonyl)hydrazinecarboxylate is a versatile compound that finds significant application in chemical synthesis. This compound is utilized as a key building block in the development of various organic molecules. Its unique structure and reactivity make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. In particular, the (S)-tert-Butyl 1-(piperidine-3-carbonyl)hydrazinecarboxylate can serve as a chiral auxiliary, enabling the asymmetric synthesis of complex molecules with high stereochemical precision. Additionally, its hydrazine moiety offers opportunities for further derivatization, allowing for the introduction of diverse functional groups and enhancing the potency or specificity of the final products. By incorporating (S)-tert-Butyl 1-(piperidine-3-carbonyl)hydrazinecarboxylate into synthetic pathways, chemists can access a wide range of structurally diverse compounds with potential applications in medicinal chemistry, materials science, and beyond.