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
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
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
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,...