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Sigma-Aldrich

(1S,2S)-N-p-Tosyl-1,2-dimesitylethylenediamine

96%

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About This Item

Empirical Formula (Hill Notation):
C27H34N2O2S
CAS Number:
1293946-41-4
Molecular Weight:
450.64
MDL number:
MFCD18785728
UNSPSC Code:
12352116
PubChem Substance ID:
329764712
NACRES:
NA.22

assay

96%

form

solid

mp

169-174 °C

SMILES string

Cc1ccc(cc1)S(=O)(=O)N[C@H]([C@@H](N)c2c(C)cc(C)cc2C)c3c(C)cc(C)cc3C

InChI

1S/C27H34N2O2S/c1-16-8-10-23(11-9-16)32(30,31)29-27(25-21(6)14-18(3)15-22(25)7)26(28)24-19(4)12-17(2)13-20(24)5/h8-15,26-27,29H,28H2,1-7H3/t26-,27-/m0/s1

InChI key

XAXZXGHDWDUHFH-SVBPBHIXSA-N

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

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Related Content

Chin Group – Professor Product Portal

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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