Welcome to LookChem.com Sign In|Join Free
  • or
Boronic acid, (2,2-diphenylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

474688-72-7

Post Buying Request

474688-72-7 Suppliers

Recommended suppliers

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

474688-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 474688-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,6,8 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 474688-72:
(8*4)+(7*7)+(6*4)+(5*6)+(4*8)+(3*8)+(2*7)+(1*2)=207
207 % 10 = 7
So 474688-72-7 is a valid CAS Registry Number.

474688-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-diphenylethenylboronic acid

1.2 Other means of identification

Product number -
Other names 2,2-diphenylvinylboronic acid

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:474688-72-7 SDS

474688-72-7Relevant academic research and scientific papers

Novel distyrylcarbazole derivatives as hole-transporting blue emitters for electroluminescent devices

Wu, Fang-Iy,Shih, Ping-I.,Yuan, Mao-Chuan,Dixit, Ajay Kumar,Shu, Ching-Fong,Chung, Zhu-Ming,Diau, Eric Wei-Guang

, p. 4753 - 4760 (2005)

We have synthesized three novel distyrylcarbazole derivatives for use as simultaneously hole-transporting and light-emitting layers in blue light-emitting diodes. Each compound, which contains a rigid carbazole core and two 2,2-diphenylvinyl end groups su

N -Heterocyclic Carbene-Catalyzed Olefination of Aldehydes with Vinyliodonium Salts to Generate α,β-Unsaturated Ketones

Rajkiewicz, Adam A.,Kalek, Marcin

, p. 1906 - 1909 (2018/04/16)

An organocatalyzed metal-free, direct olefination of aldehydes with vinyliodonium salts has been achieved by an N-heterocyclic carbene-promoted C-H bond activation. The reaction proceeds under very mild conditions, delivering a range of (hetero)aryl-vinyl ketones in good yields. The retention of the double bond configuration is uniformly observed, and the application of 2-methoxyphenyl auxiliary group in iodonium salts secures a complete selectivity of the vinyl transfer.

Binaphthalene derivatives, preparation method thereof and organic electronic device using the same

-

Page/Page column 148-149, (2014/03/26)

The present invention relates to a new binaphthalene derivative, a preparation method thereof, and an organic electronic device using the same. The binaphthalene derivative according to the present invention can perform functions of hole injection and transportation, electron injection and transportation, or light emission in an organic electronic device including an organic light-emitting device, and the device according to the present invention has excellent characteristics in terms of efficiency, drive voltage and stability, and in particular excellent effects such as a low voltage and a long life time.

APPLICATION OF TRIPHENYLENE DERIVATIVES IN ORGANIC ELECTROLUMINESCENT DEVICES

-

, (2013/02/28)

Triphenylene derivatives having a structure of formula (1) are provided. Ar represents an aromatic compound, n is 1 to 3, and each of R and R1 to R13 is a member independently selected from the group consisting of hydrogen, halo, cyano, trifluoromethyl, amino, C1-C10 alkyl, C2-C10 alkenyl, C2-C10 alkynyl, C3-C20 cycloalkyl, C3-C20 cycloalkenyl, C1-C20 heterocycloalkyl, C1-C20 heterocycloalkenyl, aryl and heteroaryl. The compound of the present invention may function as a host emitter or dopant in the emitter layer of OLED device. An OLED device is also herein provided.

NEW BINAPHTHALENE DERIVATIVES, PREPARATION METHOD THEREOF AND ORGANIC ELECTRONIC DEVICE USING THE SAME

-

Page/Page column 39, (2010/11/27)

The present invention relates to a new binaphthalene derivative, a preparation method thereof, and an organic electronic device using the same. The binaphthalene derivative according to the present invention can perform functions of hole injection and transportation, electron injection and transportation, or light emission in an organic electronic device including an organic light- emitting device, and the device according to the present invention has excellent characteristics in terms of efficiency, drive voltage and stability, and in particular excellent effects such as a low voltage and a long life time.

NOVEL IMIDAZOQUINAZOLINE DERIVATIVE, PROCESS FOR PREPARING THE SAME, AND ORGANIC ELECTRONIC DEVICE USING THE SAME

-

Page/Page column 29, (2010/11/27)

The present invention relates to a novel imidazoquinazoline derivative, a process for preparing the same, and an organic electronic device using the same. The imidazoquinazoline derivative according to the present invention serves as hole injecting, hole transporting, electron injecting, electron transporting, or a light emitting material in an organic electronic device including an organic light emitting device, and the device according to the present invention exhibits excellent characteristics in efficiency, operating voltage, and stability.

Double-spiro organic compounds and organic electroluminescent devices using the same

-

Page/Page column 48, (2010/02/15)

Disclosed are double-spiro organic compounds and an organic electroluminescence (EL) device using the same. The double-spiro organic compounds are configured to have at least three planar and substantially linear moieties, such that one planar moiety is located between two neighboring planar moieties and that the intervening planar moiety shares an atom with each of the two neighboring planar moieties. The double-spiro compounds generally have high melting point above about 300 degree C. and low crystallinity, which provide thermal stability to the organic EL devices. These organic compounds have good sublimability. They also have light-emitting, hole-injecting, hole-transporting, electron injection, electron-transporting properties and characteristics, which are favorable in the organic EL devices.

Onium Transfer Reaction of (β,β-Dialkylvinyl)(phenyl)iodonium Tetrafluoroborates via an Alkylidene Carbene Pathway: Synthesis of Group 15 Alkenyl(triphenyl)- and Group 16 Alkenyl(diphenyl)onium Salts

Ochiai, Masahito,Sueda, Takuya,Noda, Rie,Shiro, Motoo

, p. 8563 - 8567 (2007/10/03)

Group 15 1-alkenyl(triphenyl)onium (P, As, Sb) tetrafluoroborates were prepared via an onium transfer reaction of alkenyl(phenyl)iodonium tetrafluoroborates under mild conditions. The reaction involves base-induced reductive α-elimination of the iodonium salts, followed by nucleophilic trapping of the resulting free alkylidene carbenes with group 15 element-centered nucleophiles. The onium transfer reaction of the alkenyliodonium salts also produced group 16 1-alkenyl-(diphenyl)onium (S, Se, Te) tetrafluoroborates in good yields.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 474688-72-7