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N-(biphenyl-4-yl)-N-(4'-bromobiphenyl-4-yl)-9,9-dimethyl-9H-fluoren-2-amine is a complex chemical compound derived from fluorene, featuring two biphenyl moieties, a bromine substitution, and an amine group. This unique structure and potential reactivity make it a promising candidate for applications in organic synthesis, material science, and pharmaceutical research.

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  • N-(biphenyl-4-yl)-N-(4'-bromobiphenyl-4-yl)-9,9-dimethyl-9H-fluoren-2-amine

    Cas No: 1268621-99-3

  • USD $ 1.9-2.9 / Gram

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  • 1268621-99-3 Structure
  • Basic information

    1. Product Name: N-(biphenyl-4-yl)-N-(4'-broMobiphenyl-4-yl)-9,9-diMethyl-9H-fluoren-2-aMine
    2. Synonyms: N-(biphenyl-4-yl)-N-(4'-broMobiphenyl-4-yl)-9,9-diMethyl-9H-fluoren-2-aMine;9H-Fluoren-2-amine, N-[1,1'-biphenyl]-4-yl-N-(4'-bromo[1,1'-biphenyl]-4-yl)-9,9-dimethyl-
    3. CAS NO:1268621-99-3
    4. Molecular Formula: C39H30BrN
    5. Molecular Weight: 592.5662
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268621-99-3.mol
  • Chemical Properties

    1. Melting Point: 191 °C
    2. Boiling Point: 730.9±60.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.275±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -3.23±0.40(Predicted)
    10. CAS DataBase Reference: N-(biphenyl-4-yl)-N-(4'-broMobiphenyl-4-yl)-9,9-diMethyl-9H-fluoren-2-aMine(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(biphenyl-4-yl)-N-(4'-broMobiphenyl-4-yl)-9,9-diMethyl-9H-fluoren-2-aMine(1268621-99-3)
    12. EPA Substance Registry System: N-(biphenyl-4-yl)-N-(4'-broMobiphenyl-4-yl)-9,9-diMethyl-9H-fluoren-2-aMine(1268621-99-3)
  • 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: 1268621-99-3(Hazardous Substances Data)

1268621-99-3 Usage

Uses

Used in Organic Synthesis:
N-(biphenyl-4-yl)-N-(4'-bromobiphenyl-4-yl)-9,9-dimethyl-9H-fluoren-2-amine is used as a building block in organic synthesis for the creation of various complex organic molecules. Its amine group allows for further functionalization and the formation of new chemical bonds.
Used in Material Science:
In the field of material science, N-(biphenyl-4-yl)-N-(4'-bromobiphenyl-4-yl)-9,9-dimethyl-9H-fluoren-2-amine is used as a component in the development of new materials with specific properties. Its unique structure can contribute to the formation of novel polymers, coatings, or other materials with tailored characteristics.
Used in Pharmaceutical Research:
N-(biphenyl-4-yl)-N-(4'-bromobiphenyl-4-yl)-9,9-dimethyl-9H-fluoren-2-amine is utilized in pharmaceutical research as a potential precursor or intermediate in the synthesis of new drugs. Its reactivity and structural features may enable the development of innovative therapeutic agents with improved efficacy and selectivity.
Used in Chemical Research:
In chemical research, N-(biphenyl-4-yl)-N-(4'-bromobiphenyl-4-yl)-9,9-dimethyl-9H-fluoren-2-amine serves as a subject for studying the properties and reactivity of complex organic molecules. Understanding its behavior in various chemical reactions can provide insights into the design of new synthetic routes and the discovery of novel compounds.
It is important to handle N-(biphenyl-4-yl)-N-(4'-bromobiphenyl-4-yl)-9,9-dimethyl-9H-fluoren-2-amine with care and caution due to its potential hazardous properties. Proper safety measures should be taken during its synthesis, storage, and use to minimize risks.

Check Digit Verification of cas no

The CAS Registry Mumber 1268621-99-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,6,2 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1268621-99:
(9*1)+(8*2)+(7*6)+(6*8)+(5*6)+(4*2)+(3*1)+(2*9)+(1*9)=183
183 % 10 = 3
So 1268621-99-3 is a valid CAS Registry Number.

1268621-99-3Downstream Products

1268621-99-3Relevant articles and documents

Polymer, Coating Composition Comprising Same, and Organic Light Emitting Device Using Same

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Paragraph 0284-0286; 0292-0293, (2021/06/11)

The present specification relates to a polymer including a unit represented by Chemical Formula 1, a coating composition including the same, and an organic light emitting device formed using the same.

Triarylamine derivative, preparation method, application and device thereof

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Paragraph 0170-0173, (2019/10/02)

Belonging to the technical field of photoelectric material applied science and technology, the invention in particular relates to a triarylamine derivative, a preparation method and application thereof. The triarylamine derivative provided by the invention adopts triarylamine and fluorenocarbazole as the basic structural unit, and after modification, an asymmetric structure can be obtained so as to compose compounds rich in holes and with high glass transition temperature. When the compounds are used as a hole transport material, compared with the commonly used hole transport material like N,N'-diphenyl-N, N'-bis(3-methylphenyl)-1, 1'-biphenyl-4, 4'-diamine (TPD) in the prior art, the hole transport ability is significantly improved, in OLEDs, the series of compounds have significantly improved starting voltage and glass transition temperature compared with the traditional hole transport materials, and are ideal hole transport materials. In addition, when the series of compounds are used as a light-emitting layer, the efficiency of OLEDs is greatly improved, and the series of compounds are ideal light-emitting layer materials.

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND A ELECTRONIC DEVICE THEREOF

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Paragraph 0187; 0192-0194, (2019/12/31)

The present invention relates to a compound for an organic electronic element, an organic electronic element using the same, and an electronic device thereof and, more specifically, to a novel compound comprising O atom heterocycles capable of improving luminous efficiency, stability, and service life of an element, an organic electronic element using the same, and an electronic device thereof.

Heterocyclic compounds and organic electroluminescence devices thereof

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Paragraph 0101; 0104; 0105-0107, (2018/12/01)

The invention provides heterocyclic compounds and organic electroluminescence devices thereof, and belongs to the technical field of organic electroluminescence materials. Amine type groups are introduced to specific positions of a naphthalene ring, thus properly adjusting the hole mobility and achieving an objective of balancing the hole mobility and carrier mobility. An exciton composition zoneis completely in a luminescence layer. A triarylamine structure is connected to an amine group on one side of the heterocyclic compounds to increase hole transporting capability. In addition, a carbonatom is provided with two substitute groups, making structures of the compounds similar to the structure of spirofluorene, thus ensuring that the compounds have higher glass transition temperatures.A technical problem that organic electroluminescence materials in the prior art have poor luminescence properties such as low luminescence efficiency and short service lifetime is solved. Compared with the prior art, the organic electroluminescence devices based on organic electroluminescence materials and ink compositions have improved luminescence properties and the compounds are excellent OLEDmaterials.

Novel acridine compound and organic light-emitting devices thereof

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Paragraph 0089; 0090; 0091; 0092; 0093, (2017/10/23)

The invention provides a novel acridine compound and organic light-emitting devices thereof, belongs to the technical field of organic photoelectric materials, and aims to solve the technical problems of low light-emitting efficiency, high driving voltage, short service life and low light-emitting performance of the organic photoelectric material in the prior art. Compared with the prior art, the light-emitting performance of the organic light-emitting devices based on organic electroluminescence device compounds and ink compositions can be obviously improved; the novel acridine compound is used as an excellent OLED material.

NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME

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Paragraph 0065; 0066, (2017/05/18)

The present invention relates to a novel compound. More specifically, the present invention relates to a novel compound which is represented by chemical formula 1. Applied to organic light-emitting devices, the novel compound can be driven with low voltage owing to outstanding hole-injection and hole-transfer properties, and also exhibits superior electron-blocking functions. Additionally, the novel compound also achieves long lifespan, high efficiency, low voltage, and hole mobility, and prevents recrystallization of thin films due to high glass transition temperature (Tg), thereby securing excellent operational stability.COPYRIGHT KIPO 2017

An electroluminescent compound and an electroluminescent device comprising the same

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Paragraph 0289-0291; 0328-0330, (2016/10/10)

The present invention relates to an organic light emitting compound adopted to an organic electroluminescent device. The organic light emitting compound is represented by chemical formula 1 or chemical formula 2. In the case of adopting the organic light emitting compound as a phosphorescence host compound in a hole transport functional layer or a luminous layer, an organic electroluminescent device having excellent luminous characteristics such as operating voltage, brightness, long lifespan, etc.

Indole compounds and organic light-emitting device including the same

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Page/Page column 29, (2011/04/18)

Embodiments of the present invention are directed to heteroarylamine compounds wherein: each of Ar1 and Ar2 is independently selected from the group consisting of substituted and unsubstituted C6-C60 aryl groups, substituted and unsubstituted C4-C60 heteroaryl groups, and substituted and unsubstituted C6-C60 condensed polycyclic groups; X1 is selected from the group consisting of substituted and unsubstituted C6-C30 arylene groups, substituted and unsubstituted C4-C30 heteroarylene groups, and substituted and unsubstituted C6-C30 condensed polycyclic groups; and organic light-emitting devices including the heteroarylamine compounds. The organic light-emitting devices using the heteroarylamine compounds have high-efficiency, low driving voltages, high luminance and long lifespans.

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