meso-1,2-Diphenylethylenediamine

Names

[ CAS No. ]:
951-87-1

[ Name ]:
meso-1,2-Diphenylethylenediamine

[Synonym ]:
(1R,2R)-(+)-1,2-Diphenyl-1,2-ethanediamine
meso-1,2-Diphenylethylenediamine
(1R,2R)-(+)-1,2-Diphenylethylenediamine
(1R,2S)-1,2-Diphenyl-1,2-ethanediamine
(1R,2R)-1,2-Diphenylethan-1,2-diamin
(1R,2R)-1,2-Diphenylethylenediamine
(1R,2R)-(+)-1,2-Diamino-1,2-diphenylethane
(1R,2S)-1,2-diphenylethane-1,2-diamine
CH06110 MESO-1,2-DIPHENYLETHYLENEDIAMINE
(1R,2R)-1,2-Diphenyl-1,2-ethanediamine
MESO-1 2-DIPHENYLETHYLENEDIAMINE
1,2-ETHANEDIAMINE,1,2-DIPHENYL-, (1R,2S)-REL-
MFCD00274328
1,2-Ethanediamine, 1,2-diphenyl-, (1R,2S)-
(1R,2R)-(+)-1,2-Diphenyl-1,2-Ethanediamine ee
(1R,2R)-1,2-diphenylethane-1,2-diamine
1,2-Ethanediamine, 1,2-diphenyl-, (1R,2R)-

Chemical & Physical Properties

[ Density]:
1.106g/cm3

[ Boiling Point ]:
353.9ºC at 760mmHg

[ Melting Point ]:
118-122ºC

[ Molecular Formula ]:
C₁₄H₁₆N₂

[ Molecular Weight ]:
212.29000

[ Flash Point ]:
199.9ºC

[ Exact Mass ]:
212.13100

[ PSA ]:
52.04000

[ LogP ]:
3.78700

[ Index of Refraction ]:
1.619

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2921590090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2921590090

[ Summary ]:
2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Synthesis and characterisation of nickel Schiff base complexes containing the meso-1,2-diphenylethylenediamine moiety: selective interactions with a tetramolecular DNA quadruplex.

Dalton Trans. 44(7) , 3136-50, (2015)

As part of a program of preparing metal complexes which exhibit unique affinities towards different DNA structures, we have synthesised the novel Schiff base complex N,N'-bis-4-(hydroxysalicylidine)me...

Enantioseparation of 1-arylethanols via a supramolecular chiral host consisting of N-(2-naphthoyl)-L-aspartic acid and an achiral diamine.

Org. Biomol. Chem. 10(9) , 1877-82, (2012)

A supramolecular chiral host consisting of N-(2-naphthoyl)-L-aspartic acid (L-1) and meso-1,2-diphenylethylenediamine (2) is effective in enantioseparation of 1-arylethanols (up to 96% ee with 100% in...

Synthesis and antiviral activities of N-mono- and/or N,N'-di-carbamoyl and acyl derivatives of symmetrical diamines.

Chem. Pharm. Bull. 56(7) , 1052-8, (2008)

N-carbamoyl and N-acyl diamine derivatives were synthesized from symmetrical diamines by their addition to iso(thio)cyanates, cleavage reaction of acid anhydride, or N-acylation by acyl chloride. (1R,...