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150-61-8

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150-61-8 Usage

Chemical Properties

BEIGE TO LIGHT BROWN CRYSTALLINE POWDER

Uses

1,2-Dianilinoethane can forms crystalline imidazolidines with aldehydes in the presence of AcOH. N-donating ligand. Can be used as a trapping agent for aldehydes.

Synthesis Reference(s)

Synthetic Communications, 22, p. 1081, 1992 DOI: 10.1080/00397919208019300

Purification Methods

Crystallise the reagent from aqueous EtOH or MeOH. [Beilstein 12 H 543, 12 IV 986.]

Check Digit Verification of cas no

The CAS Registry Mumber 150-61-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 150-61:
(5*1)+(4*5)+(3*0)+(2*6)+(1*1)=38
38 % 10 = 8
So 150-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N2/c15-11-12-16(13-7-3-1-4-8-13)14-9-5-2-6-10-14/h1-10H,11-12,15H2

150-61-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (D0887)  N,N'-Diphenylethylenediamine  >98.0%(T)

  • 150-61-8

  • 25g

  • 720.00CNY

  • Detail
  • TCI America

  • (D0887)  N,N'-Diphenylethylenediamine  >98.0%(T)

  • 150-61-8

  • 250g

  • 4,660.00CNY

  • Detail
  • Alfa Aesar

  • (B23098)  1,2-Dianilinoethane, 97%   

  • 150-61-8

  • 5g

  • 221.0CNY

  • Detail
  • Alfa Aesar

  • (B23098)  1,2-Dianilinoethane, 97%   

  • 150-61-8

  • 25g

  • 731.0CNY

  • Detail
  • Alfa Aesar

  • (B23098)  1,2-Dianilinoethane, 97%   

  • 150-61-8

  • 100g

  • 2453.0CNY

  • Detail
  • Aldrich

  • (D27004)  N,N′-Diphenylethylenediamine  98%

  • 150-61-8

  • D27004-5G

  • 307.71CNY

  • Detail
  • Aldrich

  • (D27004)  N,N′-Diphenylethylenediamine  98%

  • 150-61-8

  • D27004-25G

  • 882.18CNY

  • Detail

150-61-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-DIANILINOETHANE

1.2 Other means of identification

Product number -
Other names 1,2-Ethanediamine, N,N‘-diphenyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:150-61-8 SDS

150-61-8Relevant articles and documents

Condensation of aniline and o-hydroxyaniline with 1,2-dibromoethane

Ismailov,Mamedov,Yusubov

, p. 284 - 285 (2004)

-

A Nanocrystal Catalyst Incorporating a Surface Bound Transition Metal to Induce Photocatalytic Sequential Electron Transfer Events

Beard, Matthew C.,Chen, Xihan,Han, Chuang,Lin, Yixiong,Martin, Jovan San,Miller, Collin,Wang, Xiaoming,Yamamoto, Nobuyuki,Yan, Yanfa,Yan, Yong,Yazdi, Sadegh,Zeng, Xianghua

supporting information, p. 11361 - 11369 (2021/08/16)

Heterogeneous photocatalysis is less common but can provide unique avenues for inducing novel chemical transformations and can also be utilized for energy transductions, i.e., the energy in the photons can be captured in chemical bonds. Here, we developed a novel heterogeneous photocatalytic system that employs a lead-halide perovskite nanocrystal (NC) to capture photons and direct photogenerated holes to a surface bound transition metal Cu-site, resulting in a N-N heterocyclization reaction. The reaction starts from surface coordinated diamine substrates and requires two subsequent photo-oxidation events per reaction cycle. We establish a photocatalytic pathway that incorporates sequential inner sphere electron transfer events, photons absorbed by the NC generate holes that are sequentially funneled to the Cu-surface site to perform the reaction. The photocatalyst is readily prepared via a controlled cation-exchange reaction and provides new opportunities in photodriven heterogeneous catalysis.

Synthesis and antioxidant properties of a novel arylamine antioxidant

Chao, Mianran,Fan, Rong,Zhang, Lulu,Wang, Xiaoyu,Shu, Qianhui,Gao, Jifeng,Chen, Lele,Gong, Peiwei,Shen, Duyi

, p. 1440 - 1445 (2021/09/02)

A novel oil-soluble arylamine antioxidant N1,N2-diphenylethane-1,2-diamine (ND) was successfully synthesized, and the potential antioxidant behavior of which had never been reported before. The structure of ND was characterized via nuclear magnetic resonance (1H NMR, 13C NMR) and electron ionization mass spectrometry. The antioxidant performance of ND and its synergistic effect with 2,6-di-tert-butyl-4-methylphenol (BHT) in di-2-ethylhexyl sebacate were evaluated by pressurized differential scanning calorimetry, thermogravimetry analysis, and hot oil oxidation test. All the results indicated that the synthesized antioxidant ND exhibited outstanding antioxidant performance and showed prominent synergistic effect with BHT in ester base oil. Furthermore, the probable synergistic anti-oxidative effect between ND and BHT was discussed, which was mainly induced by the formation of a fresh BHT radical and the regeneration of ND antioxidant.

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