670650
(1R,2R)-trans-N-Boc-1,2-cyclohexanediamine
97%
Synonym(s):
(1R)-trans-N-Boc-1,2-diaminocyclohexane
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About This Item
Recommended Products
Quality Level
Assay
≥96.5%
97%
form
solid
optical activity
[α]/D -26±2°, c = 1 in chloroform
optical purity
ee: ≥99.0%
functional group
amine
SMILES string
CC(C)(C)OC(=O)N[C@@H]1CCCC[C@H]1N
InChI
1S/C11H22N2O2/c1-11(2,3)15-10(14)13-9-7-5-4-6-8(9)12/h8-9H,4-7,12H2,1-3H3,(H,13,14)/t8-,9-/m1/s1
InChI key
AKVIZYGPJIWKOS-RKDXNWHRSA-N
Application
(1R,2R)-trans-N-Boc-1,2-cyclohexanediamine can be used as:
- An organocatalyst in the intramolecular desymmetrization of cyclohexanones to yield 2-azabicyclo[3.3.1]nonane.
- A starting material in the synthesis of a chiral nickel catalyst applicable for the Michael addition reaction of 1,3-dicarbonyl compounds to yield nitroalkenes.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Enantioselective Desymmetrization of Prochiral Cyclohexanones by Organocatalytic Intramolecular Michael Additions to α,β-Unsaturated Esters
Angewandte Chemie (International Edition in English), 54(16), 4899-4903 (2015)
Robust and Recyclable Self-Supported Chiral Nickel Catalyst for the Enantioselective Michael Addition
advanced synthesis and catalysis, 358(12), 1982-1988 (2016)
Robust and Recyclable Self-Supported Chiral Nickel Catalyst for the Enantioselective Michael Addition
Advanced Synthesis & Catalysis, 358(12), 1982-1988 (2016)
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