The following list includes a variety of chiral cyclohexane derivatives, particularly diamines and their salts, which are valuable intermediates in synthetic chemistry and catalysis:

(1s,2s)-(-)-1,2-diaminocyclohexane l-tartrate CAS:67333-70-4

(1R,2R)-(+)-1,2-Diaminocyclohexane L-tartrate cas:39961-95-0

(1S,2S)-N,N-Dimethylcyclohexane-1,2-diamine cas:894493-95-9

(1R,2R)-N,N-Dimethylcyclohexane-1,2-diamine cas:320778-92-5?

cis-1,2-Diaminocyclohexane cas:1436-59-5

cis-1,4-Cyclohexanediamine cas:15827-56-2

trans-N,N-Dimethylcyclohexane-1,2-diamine cas:67198-21-4

(1R,2R)-N,N,N`-Trimethylcyclohexane-1,2-diamine cas:79150-46-2

(1R,2R)-N1,N1,N2,N2-Tetramethylcyclohexane-1,2-diamine cas:53152-69-5

(1S,2S)-Cyclohexane-1,2-diamine cas:21436-03-3

(1S,2S)-N,N'-Dimethyl-1,2-cyclohexanediamine cas:87583-89-9

(1S,2S)-N,N,N`-Trimethylcyclohexane-1,2-diamine cas:1067631-36-0

(1S,2S)-N1,N1,N2,N2-Tetramethylcyclohexane-1,2-diamine cas:53152-68-4

(1S,2S)-(-)-1,2-Diaminocyclohexane D-tartrate cas:67333-70-4

(1R,2R)-(+)-N,N′-Di-p-tosyl-1,2-cyclohexanediaMine cas:143585-47-1

(1R,2R)-(-)-N-p-Tosyl-1,2-cyclohexanediamine cas:174291-96-4

(1S,2S)-(-)-N-(4-toluenesulphonyl)-1,2-diaminocyclohexane cas:174291-97-5

(R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) cas:138124-32-0

(S,S)-(+)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) cas:188264-84-8

(R,R)-(-)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine cas:135616-40-9

(S,S)-(+)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine cas:135616-36-3

(1R,2R)-(-)-N,N-Bis(3,5-di-t-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) cas:176763-62-5

(1R,2R)-N1,N1,N2,N2-TETRAMETHYLCYCLOHEXANE-1,2-DIAMINE cas:43148-65-8

Tert-Butyl ((1S,2R)-2-aminocyclohexyl)carbamate cas: 184954-75-4

1-Amino-2-(Boc-amino)cyclohexane cas:317595-54-3

N,N'-Dimethyl-1,2-cyclohexanediamine cas:61798-24-1

di-tert-butyl (1r,4r)-cyclohexane-1,4-diyldicarbamate cas:1388893-13-7

These compounds, primarily consisting of chiral diamines and their metal complexes, are widely used in catalysis, asymmetric synthesis, and material science. They enable the creation of enantiomerically pure compounds and play a vital role in the development of advanced chemical processes.