| Identification | Back Directory | [Name]
(1R,2R)-trans-N-Boc-1,2-Cyclohexanediamine | [CAS]
146504-07-6 | [Synonyms]
DACH-BOC
N-Boc-1R,2R-Cyclohexanediamine
(1R,2R)-N-Boc-1,2-cyclohexanediamine
(1R,2R)-N1-Boc-1,2-cyclohexanediamine
(1R)-trans-N-Boc-1,2-diaminocyclohexane
(1R,2R)-2-Amino-1-(Boc-amino)cyclohexane
(1R,2R)-1-AMINO-2-(BOC-AMINO)-CYCLOHEXANE
(1R,2R)-trans-N-Boc-1,2-Cyclohexanediamine
Trans (1R,2R)-1N-Boc-cyclohexane-1,2-diamine
N-tert-Butoxycarbonyl-R,R-1,2-diaminocyclohexane
tert-Butyl N-((1R,2R)-2-aminocyclohexyl)carbamate
(1R,2R)-Cyclohexane-1,2-diamine, N1-BOC protected
(1R,2R)-N-tert.-Butoxycarbonylcyclohexane-1,2-diamine
(1R,2R)-Cyclohexane-1,2-diamine, N1-BOC protected 95%
(1R,2R)-trans-N-Boc-1,2-cyclohexanediamine 146504-07-6
(1R,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine
(1R,2R)-(-)-N-(t-Butoxycarbonyl)-1,2-cyclohexanediamine
(1R,2R)-2-Amino-1-(tert-butoxycarbonylamino)cyclohexane
((1R,2R)-2-Aminocyclohexyl)-carbamic acid tert-butyl ester
Carbamic acid, N-[(1R,2R)-2-aminocyclohexyl]-, 1,1-dimethylethyl ester
Carbamic acid, (2-aminocyclohexyl)-, 1,1-dimethylethyl ester,(1R-trans)- | [Molecular Formula]
C11H22N2O2 | [MDL Number]
MFCD08726023 | [MOL File]
146504-07-6.mol | [Molecular Weight]
214.3 |
| Chemical Properties | Back Directory | [Melting point ]
114-115℃ | [Boiling point ]
322.1±31.0 °C(Predicted) | [density ]
1.02±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [form ]
powder to crystal | [pka]
12.26±0.40(Predicted) | [color ]
White to Almost white | [optical activity]
[α]/D -26±2°, c = 1 in chloroform | [BRN ]
7023564 | [InChIKey]
AKVIZYGPJIWKOS-RKDXNWHRSA-N |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
(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.
| [Definition]
ChEBI: (1R,2R)-trans-N-Boc-1,2-cyclohexanediamine is an amine. |
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