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730-11-0

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730-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 730-11-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 730-11:
(5*7)+(4*3)+(3*0)+(2*1)+(1*1)=50
50 % 10 = 0
So 730-11-0 is a valid CAS Registry Number.

730-11-0SDS

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-(4-methoxyphenyl)-4-nitroaniline

1.2 Other means of identification

Product number -
Other names 4'-methoxy-4-nitrodiphenylamine

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:730-11-0 SDS

730-11-0Relevant articles and documents

Design and synthesis of hyperbranched polyimide containing multi-triphenylamine moieties for memory devices

Song, Ying,Yao, Hongyan,Lv, Yunxia,Zhu, Shiyang,Liu, Shanyou,Guan, Shaowei

, p. 93094 - 93102 (2016)

A novel triamine monomer, N,N′,N′′-tris(4-methoxyphenyl)-N,N′,N′′-tris(4-phenylamino)-1,3,5-benzenetriamine, was designed and synthesized. A hyperbranched polyimide (HBPI) was prepared by reacting the triamine monomer with 4,4-(hexafluoroisopropylidene)di

Ionic liquids as designer solvents for nucleophilic aromatic substitutions

Newington, Ian,Perez-Arlandis, Juan M.,Welton, Tom

, p. 5247 - 5250 (2007)

(Chemical Equation Presented) Ionic liquids were designed to optimize the nucleophilic aromatic substitution reaction of an activated aniline with an activated arylhalide. The design was achieved by selecting the anions on the basis of calculations of the

Diarylamine Synthesis via Desulfinylative Smiles Rearrangement

Sephton, Thomas,Large, Jonathan M.,Butterworth, Sam,Greaney, Michael F.

, p. 1132 - 1135 (2022/02/09)

Diarylamines are obtained directly from sulfinamides through a novel rearrangement sequence. The transformation is transition metal-free and proceeds under mild conditions, providing facile access to highly sterically hindered diarylamines that are otherw

Diamine monomer containing tetraphenylethylene-triphenylamine structure, preparation method thereof, and application of diamine monomer in preparation of colorless polyimide

-

Paragraph 0013; 0039; 0041, (2021/05/05)

The invention discloses a diamine monomer containing a tetraphenylethylene-triphenylamine structure, a preparation method thereof, and application of the diamine monomer in preparation of colorless polyimide with an electrochromic function, and belongs to

A Tetraarylpyrrole-Based Phosphine Ligand for the Palladium-Catalyzed Amination of Aryl Chlorides

Sai, Masahiro

supporting information, p. 5422 - 5428 (2021/10/08)

A tetraarylpyrrole-based phosphine ligand L1 in combination with Pd(dba)2 provided a catalyst for the Buchwald-Hartwig amination reaction. A variety of amines were rapidly coupled with aryl chlorides at a Pd loading of 0.5 mol%. The selective monoarylation of aliphatic primary amines was achieved in the presence of 0.8 equiv. water. Comparison experiments were also conducted, which revealed that the catalytic activity of L1 is superior to representative phosphine ligands in the Pd-catalyzed C?N coupling of various amines. (Figure presented.).

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