1. Home
  2. 1-Piperazinecarboxylicacid, 3-propyl-, 1,1-dimethylethyl ester, (3R)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-Piperazinecarboxylicacid, 3-propyl-, 1,1-dimethylethyl ester, (3R)-

CCC[C@H]1NCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperazinecarboxylicacid, 3-propyl-, 1,1-dimethylethyl ester, (3R)-
CAS Number: 928025-57-4
Product Number: AG00GTWF(AGN-PC-0W1IA0)
Synonyms:
MDL No:
Molecular Formula: C12H24N2O2
Molecular Weight: 228.3312

Identification/Properties

Computed Properties
Molecular Weight:
228.336g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
228.184g/mol
Monoisotopic Mass:
228.184g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
236
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The chemical (R)-1-Boc-3-Propylpiperazine, is frequently employed in various chemical synthesis processes due to its unique structural properties. This compound serves as a valuable building block in the creation of complex molecules and pharmaceutical intermediates. In particular, it is commonly utilized in the synthesis of novel drug candidates and organic compounds with specific biological activities.Its chirality, denoted by the "R" configuration, plays a crucial role in controlling the stereochemistry of the resulting products during asymmetric synthesis. By incorporating (R)-1-Boc-3-Propylpiperazine into a reaction, chemists can selectively form enantiopure compounds, which is essential in drug development and other industries where chirality is significant.Additionally, the Boc (tert-butoxycarbonyl) protecting group present in the structure of (R)-1-Boc-3-Propylpiperazine offers a means to shield certain reactive sites within a molecule, allowing for controlled and selective manipulations in a multi-step synthesis. This protection-deprotection strategy aids chemists in achieving desired chemical transformations without unwanted side reactions, enhancing the overall efficiency of the synthetic route.Overall, the versatile application of (R)-1-Boc-3-Propylpiperazine in chemical synthesis showcases its importance as a key component in the construction of intricate molecules and the development of new therapeutic agents and functional materials.