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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-Piperazinecarboxylic acid, 3-methyl-, 1,1-dimethylethyl ester

CC1NCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Piperazinecarboxylic acid, 3-methyl-, 1,1-dimethylethyl ester
CAS Number: 120737-59-9
Product Number: AG00HFQ0(AGN-PC-0KKLB6)
Synonyms:
MDL No: MFCD03001706
Molecular Formula: C10H20N2O2
Molecular Weight: 200.278

Identification/Properties

Properties
BP:
268.7°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
200.282g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
200.152g/mol
Monoisotopic Mass:
200.152g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 1-Piperazinecarboxylic acid, 3-methyl-, 1,1-dimethylethyl ester serves as a valuable reagent for the efficient introduction of piperazine functionality into organic molecules. This compound is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its versatile nature and ability to participate in a wide range of chemical reactions. Its reactive ester group enables the formation of amide bonds, which are essential in constructing complex molecular structures. Additionally, the presence of the 3-methyl substituent offers a unique steric profile that can influence the regioselectivity and stereochemistry of the resulting products. By incorporating 1-Piperazinecarboxylic acid, 3-methyl-, 1,1-dimethylethyl ester into synthetic pathways, chemists can access diverse chemical space and tailor the properties of the final compounds for specific applications.