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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)-

1,2-Cyclohexanediamine, N,N'-dimethyl-, dihydrochloride, (1R-trans)-

CN[C@@H]1CCCC[C@H]1NC.Cl.Cl Request for Quotation
Chemical Name: 1,2-Cyclohexanediamine, N,N'-dimethyl-, dihydrochloride, (1R-trans)-
CAS Number: 70708-33-7
Product Number: AG003BGM(AGN-PC-0TYH71)
Synonyms:
MDL No: MFCD09749879
Molecular Formula: C8H20Cl2N2
Molecular Weight: 215.1638

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
215.162g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
214.1g/mol
Monoisotopic Mass:
214.1g/mol
Topological Polar Surface Area:
24.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
81.3
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312-P304+P340+P312-P363-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(1R,2R)-N,N'-Dimethyl-1,2-cyclohexanediamine Dihydrochloride is a versatile compound widely used in chemical synthesis as a chiral building block. Its unique stereochemistry makes it valuable for the asymmetric synthesis of a variety of compounds in the pharmaceutical and agrochemical industries. This compound serves as a powerful catalyst in reactions such as asymmetric hydrogenation, asymmetric addition, and asymmetric aldol reactions, enabling the production of enantiomerically pure molecules with high efficiency. Additionally, (1R,2R)-N,N'-Dimethyl-1,2-cyclohexanediamine Dihydrochloride can be utilized in the synthesis of complex biologically active molecules, making it an essential tool for chemists working in the field of organic synthesis.