Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2,2-Dinaphthylamine, also known as DI-NAPHTHALEN-2-YL-AMINE, is an organic compound with the molecular formula C20H15N. It is a useful research chemical that has been studied for its various applications in different fields.

532-18-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 532-18-3 Structure
  • Basic information

    1. Product Name: 2,2-Dinaphthylamine
    2. Synonyms: di-2-naphthylamine;DI-NAPHTHALEN-2-YL-AMINE ;N,N-Di(2-naphthyl)amine;N,N-Di(naphth2-yl)-amine;2,2-Dinaphthylamine;N-Naphthalen-2-ylnaphthalen-2-amine;N,N-Di(naphthol-yl amine;2,2'-Iminodinaphthalene
    3. CAS NO:532-18-3
    4. Molecular Formula: C20H15N
    5. Molecular Weight: 269.34
    6. EINECS: 208-529-0
    7. Product Categories: Amines
    8. Mol File: 532-18-3.mol
  • Chemical Properties

    1. Melting Point: 174 °C
    2. Boiling Point: 471 °C
    3. Flash Point: 268.5 °C
    4. Appearance: /
    5. Density: 0.9788 (rough estimate)
    6. Vapor Pressure: 4.83E-09mmHg at 25°C
    7. Refractive Index: 1.7800 (estimate)
    8. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    9. Solubility: very slightly in Ethanol
    10. Merck: 14,3267
    11. CAS DataBase Reference: 2,2-Dinaphthylamine(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2,2-Dinaphthylamine(532-18-3)
    13. EPA Substance Registry System: 2,2-Dinaphthylamine(532-18-3)
  • Safety Data

    1. Hazard Codes: Xn,N
    2. Statements: 22-43-50/53
    3. Safety Statements: 36/37-60-61
    4. RIDADR: UN 3077 9 / PGIII
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 532-18-3(Hazardous Substances Data)

532-18-3 Usage

Uses

Used in Research and Development:
2,2-Dinaphthylamine is used as a research chemical for the development and study of new compounds and materials. Its unique structure and properties make it a valuable tool in the field of chemical research.
Used in Analytical Chemistry:
2,2-Dinaphthylamine is used as a reagent for the detection of nitrites, nitrates, and chlorates. It has been cited in the literature for its application in analytical chemistry, specifically in the detection of these compounds. This application is particularly useful in environmental and industrial settings where the presence of these compounds may be of concern.

Synthesis Reference(s)

The Journal of Organic Chemistry, 24, p. 1775, 1959 DOI: 10.1021/jo01093a042

Check Digit Verification of cas no

The CAS Registry Mumber 532-18-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 532-18:
(5*5)+(4*3)+(3*2)+(2*1)+(1*8)=53
53 % 10 = 3
So 532-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H15N/c1-3-7-17-13-19(11-9-15(17)5-1)21-20-12-10-16-6-2-4-8-18(16)14-20/h1-14,21H

532-18-3SDS

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 2,2'-Dinaphthylamine

1.2 Other means of identification

Product number -
Other names N-2-Naphthalenyl-2-naphthalenamine

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:532-18-3 SDS

532-18-3Relevant articles and documents

Nitrogen-containing compound, organic electroluminescent device, and electronic device

-

Paragraph 0111-0115; 0118, (2021/01/24)

The invention provides a nitrogen-containing compound, an organic electroluminescent device and an electronic device, and belongs to the technical field of organic materials. The structure of the nitrogen-containing compound is represented by Chemical Formula 1: wherein X1, X2, Y1, Y2 are the same or different from each other and are each independently a single bond, O, S, N(R3), C(R4R5), Ge(R6R7), Si(R8R9), Se, wherein X1 and Y1 are not single bonds simultaneously and X2 and Y2 are not single bonds simultaneously.

Organic compound and electronic device and device containing the same

-

Paragraph 0216-0219; 0220-0222; 0228, (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.

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

-

Paragraph 0103; 0106-0109, (2021/06/22)

In the present invention, provided is a novel compound capable of improving luminance efficiency, stability, and service life of an element, an organic electronic element using the same, and an electronic device thereof. By using the compound of the present invention, high luminance efficiency, low driving voltages, and high heat resistance of the element can be achieved, and color purity and service life of the element can be greatly improved.

Combined KOH/BEt3Catalyst for Selective Deaminative Hydroboration of Aromatic Carboxamides for Construction of Luminophores

Li, Jinshan,Wang, Jiali,Yang, Jianguo,Yao, Wubing,Zhong, Aiguo

supporting information, p. 8086 - 8090 (2020/11/03)

The selective catalytic C-N bond cleavage of amides into value-added amine products is a desirable but challenging transformation. Molecules containing iminodibenzyl motifs are prevalent in pharmaceutical molecules and functional materials. Here we established a combined KOH/BEt3 catalyst for deaminative hydroboration of acyl-iminodibenzyl derivatives, including nonheterocyclic carboxamides, to the corresponding amines. This novel transition-metal-free methodology was also applied to the construction of Clomipramine and luminophores.

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

-

Paragraph 0105-0109; 0111; 0112-0113, (2020/06/23)

The present invention provides a novel compound capable of improving light emitting efficiency, stability, and lifespan of an element, an organic electronic element using same, and an electronic device for the same. In one aspect, the present invention provides a compound represented by the following chemical formula 1. The compounds according to the present invention by utilizing a light emitting device of high efficiency, low driving voltage, high heat resistance can be achieved, and the color purity of the device can greatly improve the service life.

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

-

Paragraph 0123; 0127-0131, (2020/06/24)

The present invention provides a novel compound capable of improving luminance efficiency, stability, and service life of an element, an organic electronic element using the same, and an electronic device thereof. By using the compound of the present invention, high luminance efficiency, low driving voltage, and high heat resistance of the element can be achieved, and color purity and service life of the element can be greatly improved.

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

-

Paragraph 0115-0119; 0121-0123, (2020/06/24)

Discloses a novel compound capable of improving the luminous efficiency, stability and lifetime of an element, and an organic electronic element, or an electronic device using the same. (by machine translation)

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

-

Paragraph 0115-0122; 0124, (2020/07/28)

The present invention provides a novel compound capable of improving light emitting efficiency, stability, and lifespan of an element, an organic electronic element using same, and an electronic device for the same. In one aspect, the present invention provides a compound represented by combination of chemical formula 1 and chemical formula 2. The compounds according to the present invention by utilizing a light emitting device of high efficiency, low driving voltage, high heat resistance can be achieved, and the color purity of the device can greatly improve the service life.

Nickel-Catalyzed C-N Cross-Coupling of Ammonia, (Hetero)anilines, and Indoles with Activated (Hetero)aryl Chlorides Enabled by Ligand Design

McGuire, Ryan T.,Paffile, Julia F. J.,Zhou, Yuqiao,Stradiotto, Mark

, p. 9292 - 9297 (2019/10/11)

The Ni(II) precatalyst (C1) featuring the phosphonite ancillary ligand Phen-DalPhos (L1) was employed in the cross-coupling of (hetero)anilines with (hetero)aryl chlorides and in the diarylation of ammonia with (hetero)aryl chlorides to afford heteroatom-dense di(hetero)arylamines. The PAd2-DalPhos precatalyst C4 provided complementary reactivity in cross-couplings of indoles with (hetero)aryl chlorides. Taken together, the demonstration of room-temperature reactivity within each of the reaction classes examined and the observation of useful chemoselectivity at low loading (≤0.5 mol % Ni) and on gram-scale distinguishes C1 and C4 from other metal catalysts (i.e., copper, palladium, nickel, or other) within the field of C-N cross-coupling chemistry.

Hydride-catalyzed selectively reductive cleavage of unactivated tertiary amides using hydrosilane

Yao, Wubing,Li, Rongrong,Yang, Jianguo,Hao, Feiyue

, p. 3874 - 3878 (2019/08/07)

The first hydride-catalyzed reductive cleavage of various unactivated tertiary amides, including the biologically active aryl-phenazine carboxamides and the challenging non-heterocyclic carbonyl functions, using low-cost hydrosilane as a reducing reagent has been developed. The novel catalyst system exhibits high efficiency and exclusive selectivity, providing the desired amines in useful to excellent yields under mild conditions. Overall, this transition metal-free process may offer a versatile alternative to currently employed expensive reducing reagents, high-pressure hydrogen or metal systems for the selective reductive cleavage of amides.

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 532-18-3