Welcome to LookChem.com Sign In|Join Free

CAS

  • or
N-(1-Naphthyl)-N-phenyl-4-bromoaniline is a chemical compound that plays a significant role in advanced organic synthesis. It is particularly recognized for its use as a reagent in the synthesis of various pharmaceutical drugs and biologically active compounds. N-(1-Naphthyl)-N-phenyl-4-bromoaniline is a member of the aromatic ethers family, which are ethers with an oxygen atom substituted by an aromatic system. It is characterized by the presence of naphthyl and phenyl groups and is valued for its electrophilic aromatic substitution, facilitated by the bromine atom. The synthetic importance of this compound makes it a subject of interest in chemical research. As with all chemicals, it is essential to handle it with care to avoid potential hazards under certain conditions.

138310-84-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • China Biggest factory Supply High Quality N-(1-Naphthyl)-N-phenyl-4-bromoaniline CAS 138310-84-6

    Cas No: 138310-84-6

  • USD $ 1.0-2.0 / Kilogram

  • 1 Kilogram

  • 5000 Kilogram/Day

  • Leader Biochemical Group
  • Contact Supplier
  • 138310-84-6 Structure
  • Basic information

    1. Product Name: N-(1-Naphthyl)-N-phenyl-4-bromoaniline
    2. Synonyms: N-(1-Naphthyl)-N-phenyl-4-bromoaniline;N-(4-Bromophenyl)-N-phenyl-1-naphthalenamine;N-(1-Naphthyl)-N-phe;N-(4-BroMophenyl)-N-phenyl-1-naphthylaMine;1-NaphthalenaMine,N-(4-broMophenyl)-N-phenyl-;1NBPPA;N-(4-Bromophenyl)-N-phenyl-1-naphthylamine;N-(1-phthyl)-N-phenyl-4-bromoaniline
    3. CAS NO:138310-84-6
    4. Molecular Formula: C22H16BrN
    5. Molecular Weight: 374.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138310-84-6.mol
  • Chemical Properties

    1. Melting Point: 91.0 to 100.0 °C
    2. Boiling Point: 502.9 °C at 760 mmHg
    3. Flash Point: 257.9 °C
    4. Appearance: /
    5. Density: 1.381
    6. Vapor Pressure: 3.06E-10mmHg at 25°C
    7. Refractive Index: 1.708
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: -1.21±0.50(Predicted)
    11. CAS DataBase Reference: N-(1-Naphthyl)-N-phenyl-4-bromoaniline(CAS DataBase Reference)
    12. NIST Chemistry Reference: N-(1-Naphthyl)-N-phenyl-4-bromoaniline(138310-84-6)
    13. EPA Substance Registry System: N-(1-Naphthyl)-N-phenyl-4-bromoaniline(138310-84-6)
  • 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: 138310-84-6(Hazardous Substances Data)

138310-84-6 Usage

Uses

Used in Pharmaceutical Synthesis:
N-(1-Naphthyl)-N-phenyl-4-bromoaniline is used as a reagent in the pharmaceutical industry for the synthesis of various drugs. Its unique structure and electrophilic properties make it a valuable component in the creation of new and effective medications.
Used in Biologically Active Compounds Synthesis:
In the field of biochemistry, N-(1-Naphthyl)-N-phenyl-4-bromoaniline is employed as a reagent for the synthesis of biologically active compounds. Its ability to participate in electrophilic aromatic substitution reactions allows for the development of molecules with potential therapeutic applications.
Used in Chemical Research:
N-(1-Naphthyl)-N-phenyl-4-bromoaniline is utilized as a substance of interest in chemical research. Its properties and reactivity contribute to the understanding of organic synthesis and the development of new chemical methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 138310-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,1 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138310-84:
(8*1)+(7*3)+(6*8)+(5*3)+(4*1)+(3*0)+(2*8)+(1*4)=116
116 % 10 = 6
So 138310-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H16BrN/c23-18-13-15-20(16-14-18)24(19-9-2-1-3-10-19)22-12-6-8-17-7-4-5-11-21(17)22/h1-16H

138310-84-6SDS

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 N-(4-bromophenyl)-N-phenylnaphthalen-1-amine

1.2 Other means of identification

Product number -
Other names 1-[N-(4-Bromophenyl)anilino]naphthalene

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:138310-84-6 SDS

138310-84-6Relevant articles and documents

Synthesis of novel thermally stable electrochromic polynorbornenes containing symmetrical diarylamine and unsymmetrical triarylamine chromophores via ring-opening metathesis polymerisation

Huang, Ying-Chi,Wang, Kun-Li,Lian, Wei-Ren,Liao, Yi-An,Liaw, Der-Jang,Lee, Kueir-Rarn,Lai, Juin-Yih

, p. 1849 - 1856 (2012)

A new electrochromic norbornene derivative (NB) containing symmetrical diphenylamine and unsymmetrical triphenylamine groups, was synthesised from norbornene amine and unsymmetrical triphenylamine-substituted bromide. NB was used to obtain unsaturated PNB via ring-opening metathesis polymerization using different Grubbs' catalysts, followed by hydrogen reduction to obtain saturated HPNB. PNB and HPNB were highly soluble in common organic solvents such as toluene, xylene, benzene, chlorobenzene, 1,2-dichlorobenzene, and tetrahydrofuran at room temperature. The glass transition temperatures (T g) of PNB and hydrogenated HPNB were 162 °C and 117 °C, respectively. The 10% weight-loss temperatures of PNB and hydrogenated HPNB were 410 °C and 450 °C, respectively. Cyclic voltammogram of HPNB film cast onto an indium-tin oxide (ITO)-coated glass substrate exhibited three reversible oxidation redox couples at 0.52, 0.85 and 1.30 V versus Ag/Ag+ in acetonitrile solution. The electrochromic characteristics of HPNB showed excellent stability and reversibility, with multi-staged colour changes from light yellow to green, dark-blue and purple as the potential changed from 0 to 1.35 V. The colour switching time and the bleaching time of the HPNB were 8.7 s and 4.3 s, respectively, at 1084 nm and 7.9 s and 3.8 s at 879 nm.

Novel hole transport materials based on N,N′-disubstituted-dihydrophenazine derivatives for electroluminescent diodes

Zheng, Zhiwen,Dong, Qingchen,Gou, Liao,Su, Jian-Hua,Huang, Jinhai

, p. 9858 - 9865 (2014)

A series of novel hole transport materials for organic light-emitting diodes (OLEDs) based on 9,14-diphenyl- 9,14-dihydrodibenzo[a,c]phenazine were synthesized and characterized by 1H NMR and 13C NMR, mass spectrometry and single crystal structure analysis methodologies. The crystal structures of three selected molecules reveal large dihedral angles between different functional units. The electro-optical properties of the materials were examined by UV-vis absorption, photoluminescence spectroscopy and cyclic voltammetry. The HOMO of the materials were between 4.83-5.08 eV, indicating a good match between the HOMO of indium tin oxide (ITO) and the HOMO of light-emitting layer, which renders the promising candidates as hole transport materials for organic light-emitting devices. In terms of the device with the structure of ITO/HTM (60 nm)/Alq3 (50 nm)/LiF (1 nm)/Al (200 nm), the device b using N,N-diphenyl-4′ -(14-phenyldibenzo[a,c]phenazin-9(14H)-yl)-[1,1′ -biphenyl]-4-amine presented a maximum luminance of 17 437 cd m-2 at 10.7 V and kept a high current efficiency (the maximum current efficiency is 2.25 cd A-1) at a high current density (>500 mA cm-2), which illustrates the exploited material possesses good hole transport and stable properties.

Amine-based compound and organic light emitting diode comprising the same

-

Paragraph 0214; 0229; 0233-0235; 0246-0247; 0252-0253, (2020/09/08)

An amine-based compound and an organic light-emitting diode including the same are provided.

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

-

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.

LUMINOGENS FOR BIOLOGICAL APPLICATIONS

-

Paragraph 213, (2018/07/05)

A compound comprises a donor and an acceptor, wherein at least one donor ( "D" ) and at least one acceptor ( "A" ) may be arranged in an order of D-A; D-A-D; A-D-A; D-D-A-D-D; A-A-D-A-A; D-A-D-A-D; and A-D-A-D-A. The compound may be selected from the group consisting of: MTPE-TP, MTPE-TT, TPE-TPA-TT, PTZ-BT-TPA, NPB-TQ, TPE-TQ-A, MTPE-BTSe, DCDPP-2TPA, DCDPP-2TPA4M, DCDP-2TPA, DCDP-2TPA4M, TTS, ROpen-DTE-TPECM, and RClosed-DTE-TPECM. The compound may be used as a probe and may be functionalized with special targeted groups to image biological species. As non-limiting examples, the compound may be used in cellular cytoplasms or tissue imaging, blood vessel imaging, in vivo fluorescence imaging, brain vascular imaging, sentinel lymph node mapping, and tumor imaging, and the compound may be used as a photoacoustic agent.

Compound Containing Ring Linked Via Carbazole and Fluorene And Organic Electronic Element Using The Same, Terminal Thereof

-

Paragraph 0247; 0248-0251, (2017/10/21)

The present invention refers to carbazole ring coupled polyarylenic backbone containing organic compound and formed electrical component, its terminal number under public affairs substrate. (by machine translation)

Compound Containing Ring Linked Via Carbazole and Fluorene And Organic Electronic Element Using The Same, Terminal Thereof

-

Paragraph 0207-0211, (2017/12/01)

Provided in the present invention are a compound containing a ring formed by bonding carbazole and fluorine, an organic electric element using the same, and a terminal thereof. The compound of the present invention can act various roles in an organic electric element and a terminal. In addition, when being applied to an organic electric element and a terminal, the compound reduces a driving voltage of the element and increases light efficiency, service life, and stability of the element.

HETEROCYCLIC COMPOUNDS AND ORGANIC LIGHT EMITTING DEVICE USING THE SAME

-

Paragraph 0184; 0185, (2016/10/10)

Disclosed are a heterocyclic compound represented by chemical formula 1 and an organic electroluminescent device including the same. According to the present invention, the heterocyclic compound can be used as a material for organic substance layers in organic electroluminescent devices.

NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME

-

Paragraph 0073-0078, (2016/11/17)

The present invention relates to a novel compound and, more particularly, to a novel compound which has excellent characteristics of hole injection and hole delivery in addition to excellent characteristics of electron shielding when the compound is applied to an organic light emitting device. Further, the compound has high triplet energy and Tg while allowing the device to have a low driving voltage, low power consumption, high efficiency, and long lifespan. The novel compound in the present invention is represented by chemical formula 1.COPYRIGHT KIPO 2016

A kind of organic electroluminescent compound

-

Paragraph 0100-0102, (2017/01/05)

The invention discloses an organic electroluminescence compound with the structure represented by formula (I). The organic electroluminescence compound has the advantages of good thermal stability high luminescence efficiency and high luminescence purity, can be used for making organic electroluminescence devices, and can be applied in the fields of organic solar cells, organic thin film transistors or organic photoreceptors.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 138310-84-6