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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)-

(R)-2-Ethylpiperazine Dihydrochloride

CC[C@H]1NCCNC1.Cl.Cl Request for Quotation
Chemical Name: (R)-2-Ethylpiperazine Dihydrochloride
CAS Number: 438050-07-8
Product Number: AG00DB79(AGN-PC-0WA2JV)
Synonyms:
MDL No:
Molecular Formula: C6H16Cl2N2
Molecular Weight: 187.1106

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
187.108g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
186.069g/mol
Monoisotopic Mass:
186.069g/mol
Topological Polar Surface Area:
24.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
63.5
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:
3
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

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Chemical Structure


The (R)-2-Ethylpiperazine dihydrochloride is a versatile compound widely employed in chemical synthesis for its ability to serve as a chiral building block. Due to its specific stereochemistry, this compound is particularly valuable in the preparation of enantiomerically pure molecules, essential in the pharmaceutical and agrochemical industries. Its chiral nature makes it a key component in the creation of various drugs and bioactive compounds where specific stereochemical configurations are crucial for their pharmacological activity. Additionally, (R)-2-Ethylpiperazine dihydrochloride is used in the development of advanced materials, such as polymers and catalysts, where precise control over molecular structure is imperative for desired properties and performance. Beyond its role in asymmetric synthesis, this compound also finds applications in the study of enzyme catalysis and as a building block in the construction of complex organic molecules with defined stereochemistry.