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9,10-Anthracenediamine, N,N,N',N'-tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 177799-11-0 Structure
  • Basic information

    1. Product Name: 9,10-Anthracenediamine, N,N,N',N'-tetraphenyl-
    2. Synonyms: 9,10-Anthracenediamine,N,N,N',N'-tetraphenyl;N,N,N',N'-tetraphenyl-anthracene-9,10-diamine;
    3. CAS NO:177799-11-0
    4. Molecular Formula: C38H28N2
    5. Molecular Weight: 512.654
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 177799-11-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 9,10-Anthracenediamine, N,N,N',N'-tetraphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9,10-Anthracenediamine, N,N,N',N'-tetraphenyl-(177799-11-0)
    11. EPA Substance Registry System: 9,10-Anthracenediamine, N,N,N',N'-tetraphenyl-(177799-11-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 177799-11-0(Hazardous Substances Data)

177799-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177799-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,7,9 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 177799-11:
(8*1)+(7*7)+(6*7)+(5*7)+(4*9)+(3*9)+(2*1)+(1*1)=200
200 % 10 = 0
So 177799-11-0 is a valid CAS Registry Number.

177799-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-N,9-N,10-N,10-N-tetraphenylanthracene-9,10-diamine

1.2 Other means of identification

Product number -
Other names N,N,N',N'-tetraphenyl-anthracene-9,10-diamine

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:177799-11-0 SDS

177799-11-0Downstream Products

177799-11-0Relevant articles and documents

Synthesis and electroluminescence property of green fluorescent dopant including anthracene and diphenylamine moiety

Jung, Hyocheol,Ryu, Jaemin,Kang, Seokwoo,Lee, Hayoon,Park, Jongwook

, p. 4799 - 4802 (2019)

We have synthesized green fluorescent emitters of N9,N9,N10,N10-tetraphenylanthracene-9, 10-diamine (TAD) and N9,N9,N10,N10-tetra-o-tolylanthracene-9, 10-diamine (oMe-

Blocking Energy-Loss Pathways for Ideal Fluorescent Organic Light-Emitting Diodes with Thermally Activated Delayed Fluorescent Sensitizers

Zhang, Dongdong,Song, Xiaozeng,Cai, Minghan,Duan, Lian

, (2018)

Organic light-emitting diodes (OLEDs) based on thermally activated delayed fluorescence-sensitized fluorescence (TSF) offer the possibility of attaining an ultimate high efficiency with low roll-off utilizing noble-metal free, easy-to-synthesize, pure org

Diboron fluorescent material as well as preparation method and device thereof OLED

-

Paragraph 0065-0066, (2019/12/08)

The invention discloses a double-boron fluorescent material, a preparation method thereof and an OLED (organic light-emitting diode) device. A molecular structure general formula of the material is shown in the description, wherein Ar is an aromatic ring

Strongly Reducing (Diarylamino)anthracene Catalyst for Metal-Free Visible-Light Photocatalytic Fluoroalkylation

Noto, Naoki,Tanaka, Yuya,Koike, Takashi,Akita, Munetaka

, p. 9408 - 9419 (2018/09/25)

Well-defined 9,10-bis(di(p-tert-butylphenyl)amino)anthracene serves as a photocatalyst for radical fluoroalkylation under visible light irradiation. The diarylamine (Donor)-anthracene (π conjugated system)-diarylamine (Donor) scaffolds are easily accessed

Synthesis method of N, N, N', N'-tetra-(4-(4'-carboxyl) biphenylyl)-9, 10-anthradiamine

-

Paragraph 0018; 0023; 0024, (2018/04/21)

The invention discloses a synthesis method of N, N, N', N'-tetra-(4-(4'-carboxyl) biphenylyl)-9, 10-anthradiamine. 9, 10-dibromoanthracene and diphenylamine are subjected to Buchwald-Hartwig aryl amination reaction, so that N, N, N', N'-tetraphenyl-9, 10-anthradiamine (A) is produced, and A is reacted with NBS, so that N, N, N', N'- tetra-(4-bromophenylacetone)-9, 10-phenylenediamine (B) is produced. The compound B is reacted with 4-methoxycarbonyl phenylboronic acid with a catalyst being added in an inert gas protection, so that N, N, N', N'-tetra-(4-(4'-methoxycarbonyl) biphenylyl)-9, 10-anthradiamine (C) is produced. The compound C is subjected to hydrolysis reaction, so that a target compound D: N, N, N', N'-tetra-(4-(4'-carboxyl) biphenylyl)-9, 10-anthradiamine is produced. Accordingto the method, a multi-benzene ring aromatic tetracarboxylic acid compound which is not reported in literatures is synthesized, and the synthesis method has the advantages that the synthesis method issimple, the synthesis cost is low, the yield is high, and the product purity is high. The target compound D is as shown in the following formula.

ORGANIC ELECTROLUMINESCENT DEVICE AND BORIC ACID AND BORINIC ACID DERIVATIVES USED THEREIN

-

Paragraph 0239; 0244; 0245, (2015/11/30)

The present invention relates to the use of aromatic boronic acid or borinic acid derivatives in organic electronic devices, in particular electroluminescent devices.

Effect of methyl substituents on the N-diaryl rings of anthracene-9,10- diamine derivatives for OLEDs applications

Yu, Yuan-Hsiang,Huang, Chien-Hsun,Yeh, Jui-Ming,Huang, Ping-Tsung

body text, p. 694 - 702 (2012/03/26)

A series of N-diaryl-anthracene-9,10-diamine derivatives with methyl substituents at meta or para position of N-diaryl rings were synthesized and used as dopants for Organic Light-Emitting Devices (OLED). The effects of substituted methyl substituents hav

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