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400607-46-7

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  • Factory Price OLED 99% 400607-46-7 Boronic acid,B-[10-(1-naphthalenyl)-9-anthracenyl]- Manufacturer

    Cas No: 400607-46-7

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400607-46-7 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 400607-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,6,0 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 400607-46:
(8*4)+(7*0)+(6*0)+(5*6)+(4*0)+(3*7)+(2*4)+(1*6)=97
97 % 10 = 7
So 400607-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H17BO2/c26-25(27)24-21-13-5-3-11-19(21)23(20-12-4-6-14-22(20)24)18-15-7-9-16-8-1-2-10-17(16)18/h1-15,26-27H

400607-46-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H52842)  10-(1-Naphthyl)anthracene-9-boronic acid, 97%   

  • 400607-46-7

  • 250mg

  • 496.0CNY

  • Detail
  • Alfa Aesar

  • (H52842)  10-(1-Naphthyl)anthracene-9-boronic acid, 97%   

  • 400607-46-7

  • 1g

  • 1588.0CNY

  • Detail

400607-46-7SDS

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 (10-(Naphthalen-1-yl)anthracen-9-yl)boronic acid

1.2 Other means of identification

Product number -
Other names 10-(1-Naphthyl)anthracene-9-boronic 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:400607-46-7 SDS

400607-46-7Relevant articles and documents

Preparation method and purification method of 9,10-substituted anthracene

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Paragraph 0044; 0055-0057, (2020/04/17)

The invention belongs to the technical field of organic synthesis and catalysis, and particularly relates to a preparation method for synthesizing 9-(naphthalene-1-yl)-10-(4-(naphthalene-2-yl)phenyl)anthracene through a five-step reaction, and a purification method. The method provided by the invention has the advantages of less catalyst dosage, high synthesis yield, less reaction by-products (impurities) (the content of removed boric acid products is less than 1%, and boric acid self-coupling products are not generated), high product purity (the HPLC purity is greater than or equal to 99.99%)and the like, and can be directly applied to OLED terminal materials of devices, and is simple, easy to operate and suitable for large-scale industrial production.

Asymmetric antracene derivatives having two naphthyl groups and organic light-emitting diode including the same

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Paragraph 0425; 0432-0434, (2019/12/25)

The present invention relates to antracene derivatives represented by [Formula A] and [Formula B], and an organic light-emitting diode including the same. Substituents X_1 to X_14, Y, and Z are the same as defined in the detailed description.

Phenanthridine Derivatives and organic light-emitting diode including the same

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Paragraph 0252; 0259-0261, (2019/11/23)

PURPOSE: A phenanthridine derivative compound is provided to obatin an organic light emitting diode with excellent light emitting property. CONSTITUTION: A phenanthridine derivative compound is denoted by chemical formula 1 or 2. An organic light emitting diode contains an anode, a cathode, and the phenanthridine derivative compounds inserted between the anode and cathode. The organic light emitting diode further contains a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, or an electron injection layer formed by monomer deposition or solution process.

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