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

Catalog Number	ACM21436033-2
CAS	21436-03-3
Structure
Description	(1S,2S)-(+)-1,2-Diaminocyclohexane, known as (+)-DCH, is an important organic compound used in a variety of applications in the field of synthetic organic chemistry. This chiral diamine is used as a starting material for the synthesis of a wide range of compounds, including drugs, pesticides, and other organic molecules. It can also be used as a catalyst for asymmetric synthesis.
Synonyms	1,2-cyclohexanediamine1,2-cyclohexanediamine, (1R,2R)-1,2-cyclohexanediamine, (1R-trans)-1,2-cyclohexanediamine, (1S,2S)-1,2-cyclohexanediamine, (1S-trans)-1,2-cyclohexanediamine, (cis)-isomer1,2-cyclohexanediamine, (trans)-(R)-isomer1,2-cyclohexanediamine, (trans)-(S)-isomer1,2-cyclohexanediamine, (trans)-isomer1,2-DACH1,2-diaminocyclohexane1,2-diaminocyclohexane, (+)-1,2-diaminocyclohexane, (-)-1,2-diaminocyclohexane, cis-1,2-diaminocyclohexane, trans-cyclohexane-1,2-diaminedachmeso-1,2-diaminocyclohexanetrans-1,2-cyclohexanediaminetrans-1,2-diaminocyclohexane
IUPAC Name	(1S,2S)-cyclohexane-1,2-diamine
Molecular Weight	114.19 g/mol
Molecular Formula	C6H14N2
Canonical SMILES	C1CCC(C(C1)N)N
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	SSJXIUAHEKJCMH-WDSKDSINSA-N
Application	(+)-DCH is used in a variety of scientific research applications, including the synthesis of drugs, pesticides, and other organic molecules. It is also used as a catalyst for asymmetric synthesis. Additionally, (+)-DCH can be used in the synthesis of peptides and peptidomimetics, as well as in the synthesis of polymers.
GHS Pictogram	Corrosive; Irritant
Isomeric SMILES	C1CC[C@@H]([C@H](C1)N)N
Properties	The biochemical and physiological effects of (+)-DCH are not well understood. However, it is believed to be nontoxic and non-carcinogenic. Additionally, it is believed to be relatively non-irritating to the skin and eyes.