684104
(1S,2S)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine dihydrochloride
95%
Synonym(s):
(1S,2S)-1,2-Bis(2,4,6-trimethylphenyl)-1,2-ethanediamine dihydrochloride
About This Item
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Assay
95%
form
solid
optical activity
[α]20/D −129°, c = 1 in H2O
mp
>300 °C
SMILES string
Cl.Cl.Cc1cc(C)c([C@H](N)[C@@H](N)c2c(C)cc(C)cc2C)c(C)c1
InChI
1S/C20H28N2.2ClH/c1-11-7-13(3)17(14(4)8-11)19(21)20(22)18-15(5)9-12(2)10-16(18)6;;/h7-10,19-20H,21-22H2,1-6H3;2*1H/t19-,20-;;/m0../s1
InChI key
HSFKFAWYBTVLDG-TULUPMBKSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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The Chin group is interested in computational and experimental approaches to understanding stereoselective recognition and catalysis. Their studies in weak forces (H-bonding, electronic and steric effects) has led to a highly efficient method for making limitless varieties of chiral vicinal diamines from the 'mother diamine' that are useful for developing stereoselective organocatalysts or transition metal-based catalysts as well as for developing drugs (Acc Chem Res (2012) p1345). The 'mother diamine' is also useful for making binol, monophos and binap analogs. The Chin group is also interested in using reversible covalent bonds for stereoselective recognition and L to D conversion of natural and non-natural amino acids (EJOC (2012) p229).
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