1S,2S-(+)-Diaminocyclohexane

CAS: 21436-03-3

Ref. 3D-FD32585

Product Information

• Name: 1S,2S-(+)-Diaminocyclohexane
• Synonyms: ((1S,2S)-2-Aminocyclohexyl)amine, (+)-(S,S)-1,2-Diaminocyclohexane, (+)-(S,S)-Dach, (+)-trans-1,2-Cyclohexanediamine, (+)-trans-1,2-Diaminocyclohexane, (1S,2S)-(+)-1,2-Aminocyclohexane, (1S,2S)-(+)-1,2-Cyclohexanediamine, (1S,2S)-(+)-Diaminocyclohexane, (1S,2S)-(+)-trans-1,2-Diaminocyclohexane, (1S,2S)-1,2-trans-Cyclohexanediamine, (1S,2S)-cyclohexane-1,2-diamine, (1S,2S)-trans-Cyclohexane-1,2-diamine, (1S-trans)-1,2-Cyclohexanediamine, (S,S)-1,2-Cyclohexanediamine, (S,S)-trans-1,2-Cyclohexanediamine, (S,S)-trans-1,2-Diaminocyclohexane, 1,2-Cyclohexanediamine, (1S,2S)-, 1,2-Cyclohexanediamine, (1S-trans)-, 1S,2S-trans-Cyclohexanediamine, Cyclohexane-(1S,2S)-diamine, S-Dach, Ss-Dac, Ss-Diaminocyclohexane, d-trans-1,2-Diaminocyclohexane, trans-(1S,2S)-1,2-Diaminocyclohexane, trans-(S,S)-1,2-Diaminocyclohexane
• CAS: 21436-03-3

Description

1S,2S-(+)-Diaminocyclohexane is a copper complex that has been reported to have anticancer activity. It has been shown to chelate metal ions and form hydrogen bonding interactions with acidic groups on the surface of cancer cells. The solubility data for 1S,2S-(+)-Diaminocyclohexane indicates that it is not soluble in water, but soluble in methanol and ethanol. Cyclic voltammetry studies indicate that the reaction mechanism for 1S,2S-(+)-Diaminocyclohexane involves electron transfer from the cyclohexane ring to a benzimidazole derivative. Linear regression analysis of carcinoma cell lines indicates that 1S,2S-(+)-Diaminocyclohexane is selective for cancer cells over normal cells.

• Brand: Biosynth

Chemical properties

• Molecular weight: 114.19 g/mol
• Formula: C₆H₁₄N₂
• Purity: Min. 95%
• Color/Form: Powder
• InChI: InChI=1S/C6H14N2/c7-5-3-1-2-4-6(5)8/h5-6H,1-4,7-8H2/t5-,6-/m0/s1
• InChI key: InChIKey=SSJXIUAHEKJCMH-WDSKDSINSA-N
• SMILES: N[C@H]1CCCC[C@@H]1N