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1,8-Pyrenediamine, N,N,N',N'-tetrakis(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142827-48-3

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142827-48-3 Usage

Type of Compound

Synthetic chemical compound

Usage

Production of polymers and plastics
Synthesis of pigment dyes
Production of pharmaceuticals
Synthesis of other organic compounds

Structure

Central 1,8-pyrenediamine core
Four 4-methylphenyl groups attached to the core

Applications

High-performance materials
Specialty chemicals

Toxicity

Toxic

Health Hazards

Skin irritation
Other potential health risks if not handled properly

Precaution

Handle with care to avoid exposure and health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 142827-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,8,2 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142827-48:
(8*1)+(7*4)+(6*2)+(5*8)+(4*2)+(3*7)+(2*4)+(1*8)=133
133 % 10 = 3
So 142827-48-3 is a valid CAS Registry Number.

142827-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,1-N,8-N,8-N-tetrakis(4-methylphenyl)pyrene-1,8-diamine

1.2 Other means of identification

Product number -
Other names -

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:142827-48-3 SDS

142827-48-3Downstream Products

142827-48-3Relevant academic research and scientific papers

COMPOUNDS FOR ELECTRONIC DEVICES

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Page/Page column 25; 26; 27, (2014/01/08)

The present invention relates to organic electroluminescent devices comprising compounds of the formula (1), in particular as blue singlet emitting materials in an electroluminescent layer.

Synthesis, structural and spectral properties of diarylamino-functionalized pyrene derivatives via Buchwald-Hartwig amination reaction

Hu, Jian-Yong,Feng, Xing,Seto, Nobuyuki,Do, Jung-Hee,Zeng, Xi,Tao, Zhu,Yamato, Takehiko

, p. 19 - 26 (2013/03/28)

A new series of diarylamino-functionalized pyrene derivatives, namely, 1-(N,N-diarylamino)-substituted pyrenes (7), isomer of 1,6-bis- and 1,8-bis(N,N-diarylamino)-substituted pyrenes (8/9) and 1,3,6,8-tetrakis(N,N- diarylamino)-substituted pyrenes (10) have been synthesized. The structures of these synthesized compounds were determined on the basis of spectral data and elemental analysis. All compounds 7-10 have bright fluorescent emissions from sky-blue to green in solution condition (λmax = 464-500 nm in CH2Cl2) and high emission efficiency (Φf = 0.84-0.96 in dichloromethane). All compounds have high thermal stability and good solubility in common organic solvents. The electronic properties of these compounds were determined by spectroscopic methods such as UV-vis absorption spectroscopy and fluorescence emission spectroscopy. Clear evidences were obtained that the longest wavelength bands of these compounds are bathochromically red-shifted as the number of the diarylamino-substituent increased.

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