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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)-

Piperazine, 2-methyl-1-(phenylmethyl)-, (2R)-

C[C@@H]1CNCCN1Cc1ccccc1 Request for Quotation
Chemical Name: Piperazine, 2-methyl-1-(phenylmethyl)-, (2R)-
CAS Number: 174671-42-2
Product Number: AG001ZVP(AGN-PC-0O4Y05)
Synonyms:
MDL No:
Molecular Formula: C12H18N2
Molecular Weight: 190.2847

Identification/Properties

Properties
BP:
281.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
190.29g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
190.147g/mol
Monoisotopic Mass:
190.147g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
164
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


As a professional chemist, I can explain the application of (R)-1-Benzyl-2-methylpiperazine in chemical synthesis. This compound, also known as (R)-BMP, is a chiral piperazine derivative that plays a significant role in organic chemistry.(R)-1-Benzyl-2-methylpiperazine is commonly used as a chiral auxiliary in asymmetric synthesis. Its unique chiral structure enables it to influence the stereochemistry of reactions it is involved in, leading to the formation of enantiomerically pure compounds. By utilizing (R)-BMP in various chemical reactions, chemists can control the stereochemical outcome of the synthesis, ultimately producing a single enantiomer of a chiral compound.Furthermore, (R)-1-Benzyl-2-methylpiperazine can serve as a valuable building block in the synthesis of biologically active molecules, pharmaceuticals, and natural products. Its chiral nature makes it a versatile tool in designing and constructing complex organic molecules with specific stereochemical properties.Overall, the use of (R)-1-Benzyl-2-methylpiperazine in chemical synthesis offers chemists a powerful strategy for achieving precise stereochemical control and accessing enantiomerically pure compounds, thereby facilitating the development of new drugs, materials, and other important chemical entities.