CAS 951-87-1|meso-1,2-Diphenylethylenediamine

Introduction:Basic information about CAS 951-87-1|meso-1,2-Diphenylethylenediamine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Namemeso-1,2-Diphenylethylenediamine
CAS Number951-87-1Molecular Weight212.29000
Density1.106g/cm3Boiling Point353.9ºC at 760mmHg
Molecular FormulaC14H16N2Melting Point118-122ºC
MSDSChineseUSAFlash Point199.9ºC
Symbol
GHS07
Signal WordWarning

Names

Name1,2-diphenylethane-1,2-diamine
SynonymMore Synonyms

Chemical & Physical Properties

Density1.106g/cm3
Boiling Point353.9ºC at 760mmHg
Melting Point118-122ºC
Molecular FormulaC14H16N2
Molecular Weight212.29000
Flash Point199.9ºC
Exact Mass212.13100
PSA52.04000
LogP3.78700
Index of Refraction1.619
InChIKeyPONXTPCRRASWKW-OKILXGFUSA-N
SMILESNC(c1ccccc1)C(N)c1ccccc1

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXi:Irritant;
Risk PhrasesR36/37/38
Safety PhrasesS26-S36
RIDADRNONH for all modes of transport
HS Code2921590090

Customs

HS Code2921590090
Summary2921590090. other aromatic polyamines and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles8

More 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,...

Synonyms

(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)-
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