C6H14N2
114.19 g/mol
Research ReagentDanger
(1S,2S)-(+)-1,2-Diaminocyclohexane
CAS21436-03-3EC606-765-2
Category
Research Reagent
Compound Class
Amine
Primary Use
Research Compound
This compound is the (1R,2R)-enantiomer of trans-1,2-diaminocyclohexane, a chiral diamine used as a building block in asymmetric catalysis. Its significance lies in its role as a ligand precursor for stereoselective synthetic methods.
building block for asymmetric catalysis
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 21436-03-3
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Referencestereoisomer of
Oxaliplatin
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pharmaceutical raw material
Referencestereoisomer of
Cis-1,2-diaminocyclohexane
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research compound
Referencestereoisomer of
(-)-trans-1,2-diaminocyclohexane
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pharmaceutical intermediate
Referencestereoisomer of
1,2-Cyclohexane-d10-diamine (cis/trans mixture)
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research compound
Safety Reference
Danger
H314Causes severe skin burns and eye damage
H317May cause an allergic skin reaction
Identifiers
IUPAC Name
trans-(1S,2S)-cyclohexane-1,2-diamine
InChIKey
SSJXIUAHEKJCMH-WDSKDSINSA-N
SMILES
C1CC[C@@H]([C@H](C1)N)N
Synonyms (21)
- (1S
- (1S,2S)-1,2-cyclohexandiamine
- (1s,2s)-diaminocyclohexane
- (S,S)-cyclohexane-1,2-diamine
- 1,2-Cyclohexanediamine #
- 1,2-Diaminocyclohexane, (+)-