USD
Links
0item(s)
Start typing to see products you are looking for.
meso-1,2-Diphenylethylenediamine, 98%|552226|951-87-1

meso-1,2-Diphenylethylenediamine, 98%

Cat. No JK552226_5_G
J&K Chemical

Product Information

Product Name
meso-1,2-Diphenylethylenediamine, 98%
Brand Name
J&K
Product Number
552226
CAS
951-87-1
Molecular Formula
C14H16N2
Molecular Weight
212.29
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
6931234
IUPAC Name
(1R,2S)-1,2-diphenylethane-1,2-diamine
InChI Key
PONXTPCRRASWKW-OKILXGFUSA-N
SMILES
C1=CC=C(C=C1)C@H(C@H(C2=CC=CC=C2)N)N

Properties

Melting Point
118-122

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

Nucleosome acidic patch-targeting binuclear ruthenium compounds induce aberrant chromatin condensation
Publication Name: Nature Communications
Publication Date: 2017-11-17
DOI: 10.1038/s41467-017-01680-4

Enantioselective Synthesis of Vicinal Diamines
Publication Name: Synfacts
Publication Date: 2017-06-19
DOI: 10.1055/s-0036-1590524

Synthesis and characterisation of nickel Schiff base complexes containing the meso-1,2-diphenylethylenediamine moiety: selective interactions with a tetramolecular DNA quadruplex.
Publication Name: Dalton transactions (Cambridge, England : 2003)
Publication Date: 2015-02-21
DOI: 10.1039/c4dt02926g

Enantioseparation of 1-arylethanols via a supramolecular chiral host consisting of N-(2-naphthoyl)-l-aspartic acid and an achiral diamine.
Publication Name: Organic & biomolecular chemistry
Publication Date: 2012-03-07
DOI: 10.1039/c2ob06475h

Oxidation of Amines
Publication Name: Science of Synthesis
Publication Date: 2010

meso-1,2-Diphenylethylenediamine, 98%

Related Product

Just added to your wishlist:
My Wishlist
You've just added this product to the cart:
Go to cart page