Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6052-15-9

Post Buying Request

6052-15-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6052-15-9 Usage

General Description

4-[2-(4-aminophenyl)ethynyl]aniline is a chemical compound with the molecular formula C14H12N2. It is a yellowish to brown powder that is commonly used in the field of organic synthesis and materials chemistry. 4-[2-(4-AMINOPHENYL)ETHYNYL]ANILINE is a type of aniline derivative and features both an ethynyl and aniline functional group. It is known for its ability to form complex structures and has applications in the development of organic electronic materials, dyes, and pharmaceuticals. Additionally, its unique structure and properties make it a valuable building block for the synthesis of various other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 6052-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6052-15:
(6*6)+(5*0)+(4*5)+(3*2)+(2*1)+(1*5)=69
69 % 10 = 9
So 6052-15-9 is a valid CAS Registry Number.

6052-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-aminophenyl)ethynyl]aniline

1.2 Other means of identification

Product number -
Other names 4,4'-diphenylethynediamine

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:6052-15-9 SDS

6052-15-9Relevant articles and documents

Single-molecule imaging of rotaxanes immobilized on glass substrates: Observation of rotary movement

Nishimura, Dai,Takashima, Yoshinori,Aoki, Hiroyuki,Takahashi, Toshiaki,Yamaguchi, Hiroyasu,Ito, Shinzaburo,Harada, Akira

, p. 6077 - 6079 (2008)

Hula hoop: The rotary movement of a chromophore-modified α-cyclodextrin (α-CD) was studied in a rotaxane structure attached to a glass substrate. The rotary movement of the α-CD was demonstrated by defocused wide-field imaging with total internal reflecti

Effect of the Linking Group on the Thermoelectric Properties of Poly(Schiff Base)s and Their Metallopolymers

Li, Jiahua,Wang, Zitong,Sun, Zelin,Xu, Linli,Wong, Wai-Yeung

supporting information, p. 1911 - 1917 (2021/06/21)

As polymer-based thermoelectric (TE) materials possess attractive features such as light weight, flexibility, low toxicity and ease of processibility, an increasing number of conducting polymers and their composites with high TE performances have been developed in recent years. Up to date, however, the research focusing on the structure-performance relationship remains rare. In this paper, two series of poly(Schiff base)s with either C=C or C≡C linker and their metallopolymers were synthesized and doped with single-walled carbon nanotubes to evaluate how the linking groups affected the TE properties of the resulting composites. Apart from the effect exerted by the morphology, experimental results suggested that the linkers played a key role in determining the band gaps, preferred molecular conformation and extent of conjugation of the polymers, which became key factors that influenced the TE properties of the resulting materials. Additionally, upon coordination with transition metal ions, the TE properties could be tuned readily.

Robust Alkyne Metathesis Catalyzed by Air Stable d2Re(V) Alkylidyne Complexes

Cui, Mingxu,Bai, Wei,Sung, Herman H. Y.,Williams, Ian D.,Jia, Guochen

supporting information, p. 13339 - 13344 (2020/09/03)

We report in this communication the first example of catalytic alkyne metathesis reactions mediated by well-defined non-d0 alkylidyne complexes. The air-stable d2 Re(V) alkylidyne complex Re4, bearing two PO-chelating ligands and a labile pyridine ligand, could catalyze homometathesis of internal alkynes with a broad substrate scope, including alcohols, amines, and even carboxylic acids. The catalyst can tolerate heating, air, and moisture in both solid and solution states, and the catalytic metathesis reactions could proceed normally in wet solvents.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 6052-15-9