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N,N-Dimethyl-4-(4-pyridinyl)aniline is a chemical compound with the molecular formula C13H15N. It is a derivative of aniline and is known for its versatility in various industrial and commercial applications.

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  • 1137-80-0 Structure
  • Basic information

    1. Product Name: N,N-Dimethyl-4-(4-pyridinyl)aniline
    2. Synonyms: 4-[4-(Dimethylamino)phenyl]pyridine;N,N-Dimethyl-4-(4-pyridinyl)aniline;Dimethyl-(4-pyridin-4-yl-phenyl)-amine
    3. CAS NO:1137-80-0
    4. Molecular Formula: C13H14N2
    5. Molecular Weight: 198.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1137-80-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 334°C at 760 mmHg
    3. Flash Point: 155.8°C
    4. Appearance: /
    5. Density: 1.066g/cm3
    6. Vapor Pressure: 0.000132mmHg at 25°C
    7. Refractive Index: 1.595
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N,N-Dimethyl-4-(4-pyridinyl)aniline(CAS DataBase Reference)
    11. NIST Chemistry Reference: N,N-Dimethyl-4-(4-pyridinyl)aniline(1137-80-0)
    12. EPA Substance Registry System: N,N-Dimethyl-4-(4-pyridinyl)aniline(1137-80-0)
  • 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: 1137-80-0(Hazardous Substances Data)

1137-80-0 Usage

Uses

Used in Dye and Pigment Production:
N,N-Dimethyl-4-(4-pyridinyl)aniline is used as a key intermediate in the synthesis of dyes and pigments, contributing to the coloration and stability of these products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, N,N-Dimethyl-4-(4-pyridinyl)aniline serves as a building block for the development of certain drugs, playing a crucial role in the creation of new medicinal compounds.
Used in Materials Science:
N,N-Dimethyl-4-(4-pyridinyl)aniline is utilized in the field of materials science, particularly in the manufacturing of polymers and plastics, where it enhances the properties of these materials.
It is important to handle N,N-Dimethyl-4-(4-pyridinyl)aniline with care, as it can be toxic if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 1137-80-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1137-80:
(6*1)+(5*1)+(4*3)+(3*7)+(2*8)+(1*0)=60
60 % 10 = 0
So 1137-80-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H14N2/c1-15(2)13-5-3-11(4-6-13)12-7-9-14-10-8-12/h3-10H,1-2H3

1137-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-4-pyridin-4-ylaniline

1.2 Other means of identification

Product number -
Other names 4'-(4-N,N-dimethylaminophenyl)pyridine

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:1137-80-0 SDS

1137-80-0Relevant articles and documents

First synthesis of novel aminophenyl pyridinium-5-(hydroxybenzoyl)-hydrazonomethyl-2-oxothiazol-3-ide derivatives and evaluation of their anticancer activities

Min, Dongguk,Han, Moon Hi,Lee, Seulki,Jung, Mankil

, p. 843 - 847 (2015)

The first total synthesis for large-scale production and anticancer activity of novel aminophenylpyridinium-5-(hydroxybenzoyl)hydrazonomethyl-2-oxothiazol-3-ide (PBHT) (1) and its derivatives are reported. The chemical structure of PBHT was unambiguously

Push-pull [2]pseudorotaxanes. Electronic control of threading by switching on/off an intramolecular charge transfer

Vella, Sarah J.,Tiburcio, Jorge,Gauld, James W.,Loeb, Stephen J.

, p. 3421 - 3424 (2006)

Addition of acid and base allows switching between two different structures in a push-pull bis(pyridinium)ethane axle, controlling its ability to form [2]pseudorotaxanes with a dibenzo-24-crown-8 ether wheel.

Fluorescent molecular rotors as sensors for the detection of thymidine phosphorylase

Petaccia, Manuela,Giansanti, Luisa,Wilson, James N.,Lee, Heajin,Battista, Sara,Mancini, Giovanna

, (2021)

Three new fluorescent molecular rotors were synthesized with the aim of using them as sensors to dose thymidine phosphorylase, one of the target enzymes of 5-fluorouracil, a potent chemotherapic drug largely used in the treatment of many solid tumors, tha

Some reactions of pyridinium salts derived from trichloromethylarenes with N- and C-nucleophiles

Belen'kii,Poddubnyi,Luiksaar,Krayushkin

, p. 1172 - 1176 (2000)

The reaction of N-(4-pyridyl)pyridinium and 4-chloropyridinium salts obtained from 1-trichloromethyl-2,4,6-trimethylbenzene and pyridine with N-nucleophiles such as piperidine and morpholine and with C-nucleophiles such as N,N-dimethylaniline and indole proceeds through hetarylation and gives the corresponding 4-substituted pyridines. N-(α,α-Dichlorobenzyl)pyridinium and N,N'-(α-chlorobenzylidene)bispyridinium salts obtained from trichloromethylbenzene do not undergo hetarylation.

Nickel-Catalyzed Amination of Aryl Chlorides with Amides

Li, Jinpeng,Huang, Changyu,Wen, Daheng,Zheng, Qingshu,Tu, Bo,Tu, Tao

, p. 687 - 691 (2021/01/09)

A nickel-catalyzed amination of aryl chlorides with diverse amides via C-N bond cleavage has been realized under mild conditions. A broad substrate scope with excellent functional group tolerance at a low catalyst loading makes the protocol powerful for synthesizing various aromatic amines. The aryl chlorides could selectively couple to the amino fragments rather than the carbonyl moieties of amides. Our protocol complements the conventional amination of aryl chlorides and expands the usage of inactive amides.

Fluorescent substrates for neurotransmitter transporters

-

, (2011/06/19)

The invention is based on the finding that IDT307 and analogs thereof are fluorescent substrates transported by several neurotransmitter transporters. Provided are methods for the analysis of neurotransmitter transport and binding using IDT307 and its ana

Highly stable 7-N,N-dibutylamino-2-azaphenanthrene and 8-N,N-dibutylamino- 2-azachrysene as a new class of second order NLO-active chromophores

Calabrese, Valentina,Quici, Silvio,Rossi, Ester,Cariati, Elena,Dragonetti, Claudia,Roberto, Dominique,Tordin, Elisa,De Angelis, Filippo,Fantacci, Simona

supporting information; experimental part, p. 8374 - 8376 (2011/02/21)

7-N,N-Dibutylamino-2-azaphenanthrene (L3), 8-N,N-dibutylamino-2- azachrysene (L4) and related Ir(i) complexes or alkylated salts show high second-order NLO responses, as determined by the EFISH technique and DFT calculations. L4

Radical Cation Probes for Photoinduced Intramolecular Electron Transfer in Metal-Organic Complexes

Wang, Yingsheng,Schanze, Kirk S.

, p. 5408 - 5419 (2007/10/03)

Two transition metal complexes of the type fac-(bpy)Re(I)(CO)3(DA)(1+) (where bpy = 2,2'-bipyridine and DA is a pyridine ligand that is substituted with a 1,2-diamine electron donor) have been prepared.The 1,2-diamine serves as a "reactive donor ligand" o

STRUCTURE-COLOUR REALATIONSHIP OF SOME NEW N-ARYLPYRIDINIUM HEMICYANINE DYES

Hutchings, Michael G.

, p. 2061 - 2068 (2007/10/02)

N-aryl derivatives of 4-(p-dimethylamino)pyridine are novel examples of donor-acceptor dyes.Para-substituents in the N-aryl group influence the spectra, such that the more electron-withdrawing lead to more bathochromic shifts.However, a 2-nitro-substituen

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