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458511

meso-1,2-Diphenylethylenediamine

Name: <I>meso</I>-1,2-Diphenylethylenediamine
Brand: ALDRICH

98%

Synonym(s):

(1R,2S)-Diaminodiphenylethane, meso-1,2-Diamino-1,2-diphenylethane, meso-1,2-Diphenyl-1,2-ethanediamine, meso-1,2-Diphenyl-1,2-ethylenediamine, meso-1,2-Diphenyldiaminoethane, meso-1,2-Diphenylethanediamine, meso-Stilbenediamine, rel-(1R,2S)-1,2-Diphenyl-1,2-ethanediamine

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About This Item

Linear Formula:

[C₆H₅CH(NH₂)-]₂

CAS Number:

951-87-1

Molecular Weight:

212.29

UNSPSC Code:

12352100

eCl@ss:

39011513

PubChem Substance ID:

24869471

NACRES:

NA.22

MDL number:

MFCD00274328

Assay:

98%

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Properties

Quality Level

100

assay

98%

mp

118-122 °C (lit.)

functional group

amine, phenyl

SMILES string

N[C@H]([C@H](N)c1ccccc1)c2ccccc2

InChI

1S/C14H16N2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10,13-14H,15-16H2/t13-,14+

InChI key

PONXTPCRRASWKW-OKILXGFUSA-N

Description

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number

0000411773

0000179263

MKBD8926V

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Stereoselective Synthesis of (1R, 2S, 3R)-Camphordiamine.

Busacca CA, et al.

The Journal of Organic Chemistry, 65(15), 4753-4755 (2000)

A novel multi-purpose enzymatic system and procedures for the rapid fluorescent determination of flavonoids in herbal pharmaceuticals and plant materials.

Irina Veselova et al.

Talanta, 171, 108-114 (2017-05-30)

The paper presents a novel multi-purpose enzymatic system and procedures for fluorescent determination of several flavonoids in herbal pharmaceuticals and plant materials after their enzyme-catalyzed oxidation by hydrogen peroxide and further derivatization with meso-1,2-diphenylethylenediamine. This system may be used for

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

Nobuko Mibu et al.

Chemical & pharmaceutical bulletin, 56(7), 1052-1058 (2008-07-02)

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,2R)-1,2-Diaminocyclohexane [(1R,2R)-1], meso-1,2-diaminocyclohexane (meso-1), (1R,2R)-1,2-diphenylethylenediamine [(1R,2R)-3], or meso-1,2-diphenylethylenediamine (meso-3) were used as the starting symmetrical

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Global Trade Item Number

SKU	GTIN
458511-1G	04061826072844
458511-5G	04061832342702