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Safety Information

732702

Sigma-Aldrich

(1S,2S)-N-p-Tosyl-1,2-di(9-anthryl)ethylenediamine

95%

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About This Item

Empirical Formula (Hill Notation):
C37H30N2O2S
Molecular Weight:
566.71
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

form

solid

mp

218-223 °C

SMILES string

Cc1ccc(cc1)S(=O)(=O)N[C@H]([C@@H](N)c2c3ccccc3cc4ccccc24)c5c6ccccc6cc7ccccc57

InChI

1S/C37H30N2O2S/c1-24-18-20-29(21-19-24)42(40,41)39-37(35-32-16-8-4-12-27(32)23-28-13-5-9-17-33(28)35)36(38)34-30-14-6-2-10-25(30)22-26-11-3-7-15-31(26)34/h2-23,36-37,39H,38H2,1H3/t36-,37-/m0/s1

InChI key

NUBJNKYOQBGKPS-BCRBLDSWSA-N

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Related Content

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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