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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-, phenylmethyl ester

CC1NCCN(C1)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 1-Piperazinecarboxylic acid, 3-methyl-, phenylmethyl ester
CAS Number: 84477-85-0
Product Number: AG004W1L(AGN-PC-05W42V)
Synonyms:
MDL No:
Molecular Formula: C13H18N2O2
Molecular Weight: 234.2942

Identification/Properties

Properties
BP:
358.024 °C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
234.299g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
234.137g/mol
Monoisotopic Mass:
234.137g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
252
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzyl 3-methylpiperazine-1-carboxylate is a versatile compound widely used in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals. This compound serves as a crucial intermediate in the synthesis of bioactive molecules due to its unique structure and reactivity. Its benzyl group provides stability and enables selective functionalization, while the piperazine ring imparts bioactivity and pharmacological properties to the final products. In medicinal chemistry, Benzyl 3-methylpiperazine-1-carboxylate is often utilized for the synthesis of potential drug candidates targeting various biological pathways. Its carboxylate functionality allows for further derivatization to tailor the compound's properties for specific applications. Additionally, this compound plays a vital role in the development of new materials and functionalized molecules through organic synthesis strategies.