|
|
| | (1S,2S)-N,N'-Dimethyl-1,2-cyclohexanediamine Basic information |
| Product Name: | (1S,2S)-N,N'-Dimethyl-1,2-cyclohexanediamine | | Synonyms: | TRANS-(1S,2S)-N,N'-BISMETHYL-1,2-CYCLOHEXANE-DIAMINE;(1S,2S)-N,N'-BISMETHYL-1,2-CYCLOHEXANE-DIAMINE;(1S,2S)-(+)-1,2-BIS(METHYLAMINO)CYCLOHEXANE;(1S)-trans-1,2-Bis(methylamino)cyclohexane, (S,S)-N,Nμ-Dimethyl-1,2-diaminocyclohexane;(S,S)-(+)-N,Nμ-Dimethyl-1,2-cyclohexanediamine;(1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamine,98%;(1S,2S)-N,N'-Dimethyl-1,2-cyclohexanediamine;(S,S)-N,N'-Dimethyl-1,2-diaminocyclohexane | | CAS: | 87583-89-9 | | MF: | C8H18N2 | | MW: | 142.24 | | EINECS: | 625-342-3 | | Product Categories: | Chiral Nitrogen;DACH&Trost Series;Isoquinolines ,Quinolines ,Quinaldines;API intermediates;Amines (Chiral);Analytical Chemistry;Chiral Building Blocks;e.e. / Absolute Configuration Determination (NMR);Enantiomer Excess & Absolute Configuration Determination;Synthetic Organic Chemistry | | Mol File: | 87583-89-9.mol |  |
| | (1S,2S)-N,N'-Dimethyl-1,2-cyclohexanediamine Chemical Properties |
| Melting point | 39-44 °C | | Boiling point | 186.8±8.0 °C(Predicted) | | alpha | 145 º (c=4.47 in chloroform) | | density | 0.902 | | refractive index | 145 ° (C=4, CHCl3) | | Fp | 74 °C | | storage temp. | 2-8°C | | pka | 11.04±0.40(Predicted) | | form | Solid | | color | Pale brown | | optical activity | [α]/D +145±5°, c = 4.47 in chloroform | | Water Solubility | Slightly soluble in water. | | BRN | 4304824 | | CAS DataBase Reference | 87583-89-9(CAS DataBase Reference) |
| Hazard Codes | C | | Risk Statements | 36/37/38-34-22 | | Safety Statements | 26-36/37/39-45 | | RIDADR | UN 3259 | | WGK Germany | 3 | | HazardClass | 8 | | PackingGroup | Ⅱ | | HS Code | 29213000 |
| | (1S,2S)-N,N'-Dimethyl-1,2-cyclohexanediamine Usage And Synthesis |
| Chemical Properties | Beige crystal | | Uses | (S,S)-(+)-N,N′-Dimethyl-1,2-cyclohexanediamine can be used:
- To synthesize derivatives of α-diazophosphonic acid, which are employed in O-H and N-H insertion reactions.
- As a starting material for the synthesis of α-chloro-α-alkylphosphonic acids.
- To prepare C2 symmetrical diamine enantiomers of C60 with chirospectrosopic properties.
| | Uses | It is employed in the synthesis of 6-substituted 1-oxoindanoyl isoleucine conjugates and modeling studies with the coi1-jaz co-receptor complex of lima bean. |
| | (1S,2S)-N,N'-Dimethyl-1,2-cyclohexanediamine Preparation Products And Raw materials |
|