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1-Naphthalenamine, 4-[(4-methylphenyl)azo]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61413-74-9

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61413-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61413-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,1 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61413-74:
(7*6)+(6*1)+(5*4)+(4*1)+(3*3)+(2*7)+(1*4)=99
99 % 10 = 9
So 61413-74-9 is a valid CAS Registry Number.

61413-74-9SDS

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 4-[(4-methylphenyl)diazenyl]naphthalen-1-amine

1.2 Other means of identification

Product number -
Other names 4-p-Tolylazo-1-naphthylamin

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:61413-74-9 SDS

61413-74-9Relevant academic research and scientific papers

Sterically enhanced 2-iminopyridylpalladium chlorides as recyclable ppm-palladium catalyst for Suzuki–Miyaura coupling in aqueous solution

Lin, Wenhua,Zhang, Liping,Ma, Yanping,Liang, Tongling,Sun, Wen-Hua

, (2021/10/20)

Sterically hindered 2-iminopyridine derivatives and their palladium chlorides complexes are designed and prepared, which efficiently promote the Suzuki–Miyaura coupling (SMC) reaction in aqueous solution. Besides the good to excellent yields and broad substrate scope, these catalysts can be reused for at least four new batches of the substrates. Spontaneous separation of coupling products in the aqueous reaction medium is the additional striking feature of this catalytic process. Furthermore, catalytic performance of palladium complexes bearing the azo-bridged phenyl groups was greatly influenced by the UV irradiation due to the cis/trans photoisomerization of azo unit of the catalysts. In conclusion, titled palladium complexes provide a green, sustainable, cost-effective, and convenient process to synthesize SMC products at multi-gram-scale reaction.

Effects of different terminal substituents on the mesomorphic behavior of some azo-Schiff base and azo-ester-based liquid crystals

Thaker,Kanojiya,Tandel

scheme or table, p. 120 - 137 (2011/05/12)

In order to investigate the influence of the terminal substitution on mesomorphism, two new series of azo-Schiff base and azo-ester liquid crystals having the following structures have been synthesized. All the compounds possess mesomorphic properties. In series A compounds A1 and A3 exhibit only a nematic mesophase, whereas compounds A2, A4, A5, A6, A7, A8, A9, and A10 exhibit a smectic as well as a nematic phase. In series B compounds B1 to B9 exhibit only a nematic mesophase, and compounds B10 and B11 exhibit a smectic as well as a nematic phase, but compound B12 exhibits only a smectic phase. All these compounds were characterized by elemental analyses and spectroscopic techniques (Fourier transform infrared [FTIR], 1H nuclear magnetic resonance [NMR], and mass spectroscopy). Their mesomorphic properties were measured by optical polarized light microscopy and differential scanning calorimetry (DSC). Copyright Taylor & Francis Group, LLC.

Mechanisms of Diazo Coupling Reactions. Part XXX. N-Diazo Coupling of p-Chloroaniline in Acetonitrile: Rate-Limiting Proton Transfer

Penton, John R.,Zollinger, Heinrich

, p. 1717 - 1727 (2007/10/02)

The N-diazo coupling of p-chloroaniline with p-chlorobenzenediazonium tetrafluoroborate in acetonitrile at 30 deg shows non-linear base catalysis by water.The results are interpreted in terms of the SE2 mechanism with rate-limiting proton loss at low base concentration; it is postulated, moreover that the reaction proceeds via transition states in which varying degrees of H-bonding from the amine and the intermediate ?-complex to different water species influence the initial step and the base catalysis.

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