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| | Trans-(1R,2R)N,N'-Dimethyl-cyclohexane-1,2-diamine Basic information | | Uses |
| Product Name: | Trans-(1R,2R)N,N'-Dimethyl-cyclohexane-1,2-diamine | | Synonyms: | trans-N,N;trans-(1R,2R)-N,N'-BisMethyl-1,2-cyclohexanedia;1,2-CyclohexanediaMine,N1,N2-diMethyl-, (1R,2R)-rel-;trans-N,N'-DiMethylcyclohexane-1,2-diaMin;rel-(1R,2R)-N1,N2-DiMethylcyclohexane-1,2-diaMine;trans-N1,N2-DiMethylcyclohexane-1,2-diaMine;(1R,2R)-rel-N1,N2-DiMethylcyclohexane-1,2-diaMine;TRANS-1,2-BIS(METHYLAMINO)CYCLOHEXANE | | CAS: | 67579-81-1 | | MF: | C8H18N2 | | MW: | 142.24 | | EINECS: | | | Product Categories: | Chiral Nitrogen;DACH&Trost Series;Chiral Reagents;Miscellaneous Reagents | | Mol File: | 67579-81-1.mol |  |
| | Trans-(1R,2R)N,N'-Dimethyl-cyclohexane-1,2-diamine Chemical Properties |
| Melting point | 4°C | | Boiling point | 83 °C / 13mmHg | | density | 0.89 | | refractive index | n20/D1.472(lit.) | | Fp | 60℃ | | storage temp. | Keep in dark place,Inert atmosphere,2-8°C | | pka | 11.04±0.40(Predicted) | | form | liquid | | color | colorless to pale yellow | | Sensitive | air sensitive | | InChIKey | JRHPOFJADXHYBR-HTQZYQBOSA-N | | CAS DataBase Reference | 67579-81-1(CAS DataBase Reference) |
| Hazard Codes | C | | Risk Statements | 36/37/38-34-22 | | Safety Statements | 26-36/37/39-45 | | RIDADR | 2735 | | WGK Germany | 3 | | HazardClass | 8 | | PackingGroup | Ⅱ | | HS Code | 2921309990 |
| | Trans-(1R,2R)N,N'-Dimethyl-cyclohexane-1,2-diamine Usage And Synthesis |
| Uses | Trans-(1R,2R)N,N'-Dimethyl-cyclohexane-1,2-diamine used with CuI to form a general and highly efficient catalyst for the N-amidation of aryl and heteroaryl iodides, bromides and in some cases, unactivated aryl chlorides. The catalyst system is also used for the N-arylation of indoles. | | Description | Trans-(1R,2R)N,N'-Dimethyl-cyclohexane-1,2-diamine is a useful research chemical for organic synthesis and other chemical processes. | | Uses | trans-N,N′-dimethylcyclohexane-1,2-diamine can be used as a ligand in the synthesis of the following products via copper catalyzed C-N coupling reactions:
- vinylsulfoximines obtained from NH sulfoximes and vinyl bromides
- N-arylpyridones obtained via reaction between 2-substituted pyridines and aryl halides
- N-aryl amines obtained via reaction between amines and aryl iodides/aryl bromides
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| | Trans-(1R,2R)N,N'-Dimethyl-cyclohexane-1,2-diamine Preparation Products And Raw materials |
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