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Home > Encyclopedia > 2,2′-Ethylenedianiline

2,2′-Ethylenedianiline

2,2′-Ethylenedianiline structure

2,2′-Ethylenedianiline 

structure
  • CAS No:

    34124-14-6

  • Formula:

    C14H16N2

  • Chemical Name:

    2,2′-Ethylenedianiline

  • Synonyms:

    Benzenamine,2,2′-(1,2-ethanediyl)bis-;α,α′-Bi-o-toluidine;2,2′-(1,2-Ethanediyl)bis[benzenamine];2,2′-Diaminobibenzyl;2,2′-Diaminodibenzyl;NSC 159119;2,2′-Ethylenedianiline;2-(2-(2-Aminophenyl)ethyl)benzenamine;2,2′-(Ethane-1,2-diyl)dianiline;2-[2-(2-Aminophenyl)ethyl]aniline

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

Description

BROWN POWDER

2,2′-Ethylenedianiline Basic Attributes

212.29

212.29

251-837-5

159119

DTXSID50187714

2921590090

Characteristics

52

2.8

1.132g/cm3

241-242 °C

342.14°C (rough estimate)

221ºC

1.654

Safety Information

20/21/22

36/37

Xn

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

2,2′-Ethylenedianiline Use and Manufacturing

A. Preparation of Supported Nickel Catalyst Take 4.75g of nickel chloride hexahydrate in a 25ml round bottom flask, dissolved in 15ml of deionized water, Add 20g of neutral alumina, stir with ultrasound and dry overnight. Weigh 0.3g sodium borohydride, Configured to 800ml 0.01mol / L solution, 5g precursor was added to a 1L flask, added with mechanical stirring, Sodium borohydride aqueous solution, the product was filtered and dried to obtain the desired catalyst.B. Preparation of 2, 2-diamino bibenzylTake a capacity of 10ml round bottom flask, add 300mg o-nitrobenzyl chloride, 300mg catalyst, 2ml deionized water, 2ml of 60percent hydrazine hydrate was slowly added dropwise under magnetic stirring until completely added and stirred at room temperature for 20 minutes, The product is obtained. After the product was extracted with ethyl acetate, it was found by GCMS that about 51percent of the target product was obtained. The catalyst was washed with water and ethanol three times and then dried for use.

Computed Properties

Molecular Weight:212.29
XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:212.131348519
Monoisotopic Mass:212.131348519
Topological Polar Surface Area:52
Heavy Atom Count:16
Complexity:183
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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