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N-[1,1'-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1198395-24-2 Structure
  • Basic information

    1. Product Name: N-[1,1'-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-2-amine
    2. Synonyms: Biphenyl-2-yl-(9,9-diMethyl-9H-fluoren-2-yl)-aMine;N-(bipheny-2-yl)-9,9-diMethyl-9H-fluoren-2-aMine;9,9-dimethyl-N-(2-phenylphenyl)fluoren-2-amine;9H-Fluoren-2-amine, N-[1,1'-biphenyl]-2-yl-9,9-dimethyl-;N-[1,1'-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-2-amine;2-(2-Biphenylyl)amino-9,9-dimethylfluorene;N-(2-Biphenyl)-9,9-dimethylfluorene-2-amine
    3. CAS NO:1198395-24-2
    4. Molecular Formula: C27H23N
    5. Molecular Weight: 361.47822
    6. EINECS: 1312995-182-4
    7. Product Categories: OLED materials,pharm chemical,electronic
    8. Mol File: 1198395-24-2.mol
  • Chemical Properties

    1. Melting Point: 118.0 to 124.0 °C
    2. Boiling Point: 531.4±39.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.136
    6. Vapor Pressure: 0-0Pa at 20-50℃
    7. Refractive Index: N/A
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 0.28±0.40(Predicted)
    11. CAS DataBase Reference: N-[1,1'-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-2-amine(CAS DataBase Reference)
    12. NIST Chemistry Reference: N-[1,1'-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-2-amine(1198395-24-2)
    13. EPA Substance Registry System: N-[1,1'-Biphenyl]-2-yl-9,9-dimethyl-9H-fluoren-2-amine(1198395-24-2)
  • 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: 1198395-24-2(Hazardous Substances Data)

1198395-24-2 Usage

Chemical Properties

off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 1198395-24-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,3,9 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1198395-24:
(9*1)+(8*1)+(7*9)+(6*8)+(5*3)+(4*9)+(3*5)+(2*2)+(1*4)=202
202 % 10 = 2
So 1198395-24-2 is a valid CAS Registry Number.

1198395-24-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 9,9-dimethyl-N-(2-phenylphenyl)fluoren-2-amine

1.2 Other means of identification

Product number -
Other names -([1,1'-Biphenyl]-2-yl)-9,9-dimethyl-9-fluoren-2-amine

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:1198395-24-2 SDS

1198395-24-2Downstream Products

1198395-24-2Relevant articles and documents

Organic compound and electronic device and device containing the same

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Paragraph 0216-0219; 0220-0222; 0226, (2021/09/11)

The invention relates to the technical field of organic electroluminescent materials, in particular to an organic electroluminescent material 9 with 10 -9 dihydro 9 -10 -dimethyl and oxanthrene and arylamine groups, an electronic device containing the compound and a device. The organic electroluminescent device has lower driving voltage. Higher luminous efficiency and longer service life.

Tetraphenyl ethylene type compound, application thereof and electronic device using same

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Paragraph 0062-0066, (2021/01/29)

The invention discloses a tetraphenyl ethylene type compound, application thereof and an electronic device using the tetraphenyl ethylene type compound. The structural general formula of the tetraphenyl ethylene type compound is shown as the following for

Compound, application thereof and device comprising compound

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Paragraph 0060-0064, (2021/01/04)

The invention relates to a compound, application thereof and a device comprising the compound. The organic compound has a structure represented by the following formula (1): R1, R2 and R3 are each independently selected from one of hydrogen, halogen, C1-C12 alkyl groups, C3-C12 cycloalkyl groups, C1-C12 alkoxy groups, substituted or unsubstituted C6-C30 arylamino groups, substituted or unsubstituted C3-C30 heteroarylamino groups, substituted or unsubstituted C6-C30 aryl groups, and substituted or unsubstituted C3-C30 heteroaryls; and a, b, and c are each independently an integer of 0-4. When the compound provided by the invention is used as a hole transport layer or an electron blocking layer material in an OLED device, excellent device performance and stability are shown. The invention also discloses an organic light-emitting device adopting the compound with the general formula.

Fluorenyl organic electroluminescent compound and organic electroluminescent device (by machine translation)

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Paragraph 0210-0211, (2020/08/25)

The invention discloses a fluorene-based organic electroluminescent compound and an organic electroluminescent device, and the structural formula is as shown in the specification. Wherein, L1. L2, R1 are the same or different and are each independently a linear or branched alkyl group of R2, a substituted or unsubstituted C1 - C30 alkyl, substituted or unsubstituted C2 - C30 C3 - C30 heteroaromatic hydrocarbon group; A is a substituted or unsubstituted C6 - C30 C2 - C30 heteroaromatic hydrocarbon group; the starting voltage of the device is reduced; the power consumption of the device is relatively reduced, so that the service life of the device is correspondingly improved C2 - C30 C5 - C60 C6 - C30. (by machine translation)

Organic compound containing dibenzocycloheptene, preparation method thereof and application thereof

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Paragraph 0096-0098; 0105, (2020/03/13)

The invention relates to an organic compound containing dibenzocycloheptene, a preparation method thereof and application thereof, and belongs to the technical field of semiconductors. The structure of the compound is shown as the general formula (1) shown in the specification. The invention also discloses a preparation method and application of the compound. The compound has strong hole-transporting ability, and improved hole injection and transport performance at an appropriate HOMO energy level; and at an appropriate LUMO energy level, the compound also plays a role of electron blocking andenhances the exciton recombination efficiency in a light-emitting layer. When used as the material of a light-emitting functional layer of an OLED light-emitting device, the compound when in combination with a branched chain within the scope of the present invention can effectively improve the exciton utilization rate and the radiation efficiency.

Compound for preparing organic photoelectric devices

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Paragraph 0056-0060, (2020/08/18)

The invention belongs to the technical field of organic photoelectric materials, and particularly relates to a compound for preparing organic photoelectric devices. The structural formula is shown inthe specification. The series of organic materials containing xanthone, thiazolone, acridone and other structures synthesized in the invention can have wide ultraviolet absorption through modificationof different groups, and can be used as organic materials or stabilizers with high oxygen, heat, light and ultraviolet stability, especially organic electronic and photoelectric materials or organicelectronic material stabilizers. The material can be used as a hole type charge transport material in the field of OLED display.

Compound containing silafluorenyl and fluorenyl structures and electroluminescent device containing compound

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Paragraph 0102-0104, (2020/06/09)

Disclosed is a novel compound containing a silafluorenyl structure and a fluorenyl structure. The compound is a triarylamine compound containing silafluorenyl and fluorenyl at the same time, and can be used as a hole-transport material and an electron blocking material in an electroluminescent device. The novel compounds can provide better comprehensive device performance. An electroluminescent device comprising the compound and a compound formula are also disclosed.

Luminescent material and application thereof

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Paragraph 0089-0091, (2020/06/17)

The invention discloses a novel organic compound, which has a structure represented by the following formula (I), wherein Ar, Ar, Ar and Ar are respectively and independently selected fromone of substituted or unsubstituted C6-C30 aryl, substituted or unsubstituted C6-C30 condensed aryl and substituted or unsubstituted C3-C30 heteroaryl, L, L, L and L are respectively andindependently selected from one of a single bond, substituted or unsubstituted C6-C30arylene, substituted or unsubstituted C6-C30 heteroarylene and substituted or unsubstituted C6-C30 condensed arylene, and the L-Ar, the L-Ar, the L-Ar and the L-Ar do not select the same substituent group at the same time. When the compound provided by the invention is used as a hole transport material in an OLED device, excellent device performance and stability are shown. The invention also discloses an organic light-emitting device adopting the compound with the general formula.

COMPOUND AND ORGANIC ELECTRONIC DEVICE PREPARED THEREWITH

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Paragraph 0104; 0105; 0106; 0107, (2019/04/30)

PROBLEM TO BE SOLVED: To provide a novel compound, and a hole transport body and an organic electronic device with improved OLED current efficiency. SOLUTION: The present invention provides a compound illustrated by the following formula. SELECTED DRAWING

Organic electroluminescence material and organic electroluminescence device with material

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Paragraph 0106-0108, (2019/10/01)

The invention relates to an organic electroluminescence material and an organic electroluminescence device with the material. Novel aryl group-dihydrophenanthrene is introduced as one of core groups,a dihydrophenanthrene derivative is obtained and has hig

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