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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)-

(2R,5R)-1,6-diphenylhexane-2,5-diamine dihydrochloride

N[C@@H](Cc1ccccc1)CC[C@H](Cc1ccccc1)N.Cl.Cl Request for Quotation
Chemical Name: (2R,5R)-1,6-diphenylhexane-2,5-diamine dihydrochloride
CAS Number: 1247119-31-8
Product Number: AG000MNC(AGN-PC-0WCYA1)
Synonyms:
MDL No:
Molecular Formula: C18H26Cl2N2
Molecular Weight: 341.3184

Identification/Properties

Computed Properties
Molecular Weight:
341.32g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
7
Exact Mass:
340.147g/mol
Monoisotopic Mass:
340.147g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
216
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (2R,5R)-1,6-diphenylhexane-2,5-diamine dihydrochloride serves as a valuable reagent in chemical synthesis processes. It has shown significant utility in asymmetric catalysis, enabling the selective formation of chiral compounds. This compound's unique structure and stereochemistry make it particularly useful in the production of enantiomerically pure molecules, a crucial aspect in the pharmaceutical and agrochemical industries. Furthermore, (2R,5R)-1,6-diphenylhexane-2,5-diamine dihydrochloride's ability to facilitate diverse bond-forming reactions and its compatibility with a wide range of functional groups further enhance its appeal in synthetic applications, making it a versatile and essential tool for organic chemists.