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N,N-diphenyl-9H-carbazol-3-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 883224-26-8 Structure
  • Basic information

    1. Product Name: N,N-diphenyl-9H-carbazol-3-amine
    2. Synonyms: N,N-diphenyl-9H-carbazol-3-amine
    3. CAS NO:883224-26-8
    4. Molecular Formula: C24H18N2
    5. Molecular Weight: 334.41312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 883224-26-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 543.6±23.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.251±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 17.47±0.30(Predicted)
    10. CAS DataBase Reference: N,N-diphenyl-9H-carbazol-3-amine(CAS DataBase Reference)
    11. NIST Chemistry Reference: N,N-diphenyl-9H-carbazol-3-amine(883224-26-8)
    12. EPA Substance Registry System: N,N-diphenyl-9H-carbazol-3-amine(883224-26-8)
  • 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: 883224-26-8(Hazardous Substances Data)

883224-26-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 883224-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,2,2 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 883224-26:
(8*8)+(7*8)+(6*3)+(5*2)+(4*2)+(3*4)+(2*2)+(1*6)=178
178 % 10 = 8
So 883224-26-8 is a valid CAS Registry Number.

883224-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diphenyl-9H-carbazol-3-amine

1.2 Other means of identification

Product number -
Other names 9H-Carbazol-3-amine,N,N-diphenyl

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:883224-26-8 SDS

883224-26-8Downstream Products

883224-26-8Relevant articles and documents

Triarylboron-Based Fluorescent Organic Light-Emitting Diodes with External Quantum Efficiencies Exceeding 20 %

Suzuki, Katsuaki,Kubo, Shosei,Shizu, Katsuyuki,Fukushima, Tatsuya,Wakamiya, Atsushi,Murata, Yasujiro,Adachi, Chihaya,Kaji, Hironori

, p. 15231 - 15235 (2015)

Triarylboron compounds have attracted much attention, and found wide use as functional materials because of their electron-accepting properties arising from the vacant p orbitals on the boron atoms. In this study, we design and synthesize new donor-accept

Compound for organic luminescence and application of compound

-

Paragraph 0041; 0046-0047; 0048-0049, (2021/06/22)

The invention relates to a compound for organic luminescence. The structure of the compound is shown as a formula (I), Ar1 and Ar2 are respectively and independently selected from hydrogen or an electron donating structural unit, but Ar1 and Ar2 are not hydrogen at the same time. The compound for organic luminescence is a thermally activated delayed fluorescent material with aggregation-induced emission property, is simple in process, easy to purify and high in yield, and can adjust the thermal property, luminescence property and the like of a final product by introducing different groups. When the material is applied to an organic electroluminescent device as a luminescent layer material, the manufactured device has long service life and can meet the requirements of panel manufacturing enterprises.

Boron-containing organic electroluminescent material and application thereof in organic electroluminescent device

-

Page/Page column 0084-0089; 0124-0125, (2020/06/20)

The invention discloses a boron-containing organic electroluminescent material and application thereof in an organic electroluminescent device, the compound comprises boron groups, and the compound has strong group rigidity, and has the characteristics of

Arylamine compound and organic electroluminescent device thereof

-

Paragraph 0104-0106; 0123-0128, (2020/10/20)

The invention provides an arylamine compound and an organic electroluminescent device thereof, and belongs to the technical field of organic photoelectric materials. In order to achieve better light emission inside a light-emitting layer so as to improve

METHOD FOR PRODUCING (DIARYLAMINO) CARBAZOLE

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Paragraph 0043-0093, (2019/09/19)

PROBLEM TO BE SOLVED: To provide a method for producing (diarylamino) carbazole in one stage, with high selectivity and high efficiency. SOLUTION: Halocarbazole represented by general formula (1) (where X is a halogen atom. n is an integer of 1 to 4) is r

ORGANIC LIGHT-EMITTING DIODE MATERIALS

-

Paragraph 0547; 0548; 0550, (2018/08/09)

Described herin are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moeity D, each moiety D is covalently attached to either the moeity B or the moeity A, and each B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D and B are defined herein.

Organic light-emitting diode materials

-

Paragraph 0351; 0352; 0355; 0373; 0385, (2017/07/26)

Described herein are molecules for use in organic light emitting diodes. Example molecules comprise at least one acceptor moiety A, at least one donor moiety D, and optionally one or more bridge moieties B. Each moiety A is covalently attached to either the moiety B or the moiety D, each moiety D is covalently attached to either the moiety B or the moiety A, and each moiety B is covalently attached to at least one moiety A and at least one moiety D. Values and preferred values of moieties A, D, and B are defined herein.

ORGANIC LIGHT-EMITTING DEVICE

-

Paragraph 0255; 0256, (2017/04/12)

An organic light-emitting device including a first electrode; a second electrode; and an organic layer disposed between the first electrode and the second electrode, wherein the organic layer comprises an emission layer, and wherein the organic layer comprises a first compound represented by Formula 1 and a second compound having the lowest excited triplet energy level greater than 2.73 electron volts: wherein in Formula 1, R11 to R33 are the same as described in the specification.

A carbazole compound and its preparation method, the organic electroluminescent device (by machine translation)

-

Paragraph 0133; 0134; 0135; 0136; 0137; 0138, (2016/10/10)

This invention has offered a kind of carbazole compound, the carbazole compound of formula (1) structure. Compared with the prior art, the present invention provides the carbazole compound is introduced in the carbazole compound is connected with the ethe

METHOD FOR PRODUCING CARBAZOLE COMPOUND HAVING TERTIARY AMINO GROUP, AND THE COMPOUND

-

Paragraph 0063; 0065; 0082, (2018/11/03)

PROBLEM TO BE SOLVED: To provide a production method which can provide a carbazole compound having a tertiary amino group in high yield with suppressed formation of by-products, and which can simplify the production process. SOLUTION: The carbazole compound having a tertiary amino group is produced by using: a step of introducing a tertiary amino group into a compound comprising a 9-butoxycarbonylcarbazole structure; and a step of eliminating the butoxycarbonyl group from the compound. COPYRIGHT: (C)2016,JPOandINPIT

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