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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)-

(S)-1-N-BOC-2-METHYL PIPERAZINE-HCl

C[C@H]1CNCCN1C(=O)OC(C)(C)C.Cl Request for Quotation
Chemical Name: (S)-1-N-BOC-2-METHYL PIPERAZINE-HCl
CAS Number: 960283-58-3
Product Number: AG0068Z1(AGN-PC-0WA2TY)
Synonyms:
MDL No:
Molecular Formula: C10H21ClN2O2
Molecular Weight: 236.7389

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.74g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
236.129g/mol
Monoisotopic Mass:
236.129g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
211
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-tert-Butyl 2-methylpiperazine-1-carboxylate hydrochloride is a versatile compound used in chemical synthesis as a chiral building block. Its asymmetric nature makes it an invaluable tool in the development of various pharmaceuticals and fine chemicals. This compound can be utilized as a key intermediate in the synthesis of complex molecules, especially in the formation of chiral compounds where stereochemistry is crucial. Its unique structural properties enable the selective formation of enantiomerically pure products, making it highly sought after in the field of organic synthesis. Additionally, (S)-tert-Butyl 2-methylpiperazine-1-carboxylate hydrochloride offers enhanced control over molecular orientation and reactivity, leading to efficient and selective synthetic pathways. The compound's compatibility with a wide range of functional groups further expands its utility in the creation of diverse chemical structures with specific biological activities.