CAS 21436-03-3

(+)-trans-1,2-Diaminocyclohexane

Description:

(+)-trans-1,2-Diaminocyclohexane, with the CAS number 21436-03-3, is an organic compound characterized by its cyclic structure and the presence of two amino groups (-NH2) attached to a cyclohexane ring. This compound is a chiral molecule, existing in two enantiomeric forms, with the (+) designation indicating the specific optical activity of the trans isomer. The trans configuration refers to the spatial arrangement of the amino groups, which are positioned on opposite sides of the cyclohexane ring, influencing its steric and electronic properties. This compound is often utilized in coordination chemistry and as a ligand in metal complexes due to its ability to form stable chelates. Additionally, it has potential applications in pharmaceuticals and materials science, where its unique structural features can impart specific functionalities. The presence of the amino groups also allows for hydrogen bonding, which can affect solubility and reactivity in various chemical environments. Overall, (+)-trans-1,2-Diaminocyclohexane is a versatile compound with significant implications in both theoretical and applied chemistry.

Formula: C₆H₁₄N₂

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]1[C@@H](N)CCCC1

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
• (1S,2S)-(+)-1,2-DIAMINOCYCLOHEXANE
• (1S,2S)-1,2-DIAMINOCYCLOHEXANE
• (1S,2S)-Cyclohexane-1,2-Diamin
• (1S,2S)-(+)-1,2-DIAMINOCYCLOHEXANE 98%
• (1S)-TRANS-1,2-DIAMINOCYCLOHEXANE
• (1S)-trans-1,2-Cyclohexanediamine, (1S)-trans-1,2-Diaminocyclohexane
• (1S,2S)-(+)-1,2-Diaminocyclohexane,99%(S,S)-DACH
• (1S,2S)-(+)-1,2-DIAMINOCYCLOHEXANE (S,S)-DACH

(1S,2S)-(+)-1,2-Cyclohexanediamine

CAS: 21436-03-3

Formula: C₆H₁₄N₂

Purity: >98.0%(GC)(T)

Color and Shape: White or Colorless to Yellow to Orange powder to lump to clear liquid

Molecular weight: 114.19

Ref: 3B-C1448

(1S,2S)-(+)-1,2-Diaminocyclohexane, 98%

CAS: 21436-03-3

For synthesis of optically active products This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a

Formula: C₆H₁₄N₂

Purity: 98%

Color and Shape: Colorless to white to pale cream to cream to yellow, Crystals or powder or crystalline powder or fused solid

Molecular weight: 114.19

Ref: 02-L14072

(1S,2S)-(+)-1,2-Diaminocyclohexane, 99% (S,S)-DACH

CAS: 21436-03-3

(1S,2S)-(+)-1,2-Diaminocyclohexane, 99% (S,S)-DACH

Formula: C₆H₁₄N₂

Purity: 99%

Color and Shape: white pwdr.

Molecular weight: 114.19

Ref: 08-07-0335

(1S,2S)-Cyclohexane-1,2-diamine

CAS: 21436-03-3

Formula: C₆H₁₄N₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 114.1888

Ref: IN-DA003BIL

(1S,2S)-(+)-1,2-Diaminocyclohexane

CAS: 21436-03-3

(1S,2S)-(+)-1,2-Diaminocyclohexane

Formula: C₆H₁₄N₂

Purity: 96%

Color and Shape: colorless solid

Molecular weight: 114.19g/mol

Ref: 54-OR307157

1S,2S-(+)-Diaminocyclohexane

CAS: 21436-03-3

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.

Formula: C₆H₁₄N₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 114.19 g/mol

Ref: 3D-FD32585

(S,S)-(+)-1,2-Diaminocyclohexane

CAS: 21436-03-3

Formula: C₆H₁₄N₂

Purity: 98.0%

Color and Shape: Solid, Crystalline Powder

Molecular weight: 114.192

Ref: 10-F012706