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1,4-Benzenediamine,N1,N4-bis(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24413-67-0

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24413-67-0 Usage

Chemical structure

1,4-Benzenediamine, N1,N4-bis(4-methoxyphenyl)-

Appearance

White to off-white crystalline solid

Solubility

Slightly soluble in water, soluble in organic solvents

Uses

a. Developer in color photography
b. Intermediate in the synthesis of dyes and pigments

Toxicity

Considered toxic

Health hazards

Can cause irritation to skin, eyes, and respiratory system

Carcinogenic potential

Identified as a potential carcinogen

Precautions

Avoid exposure to minimize health risks

Check Digit Verification of cas no

The CAS Registry Mumber 24413-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,1 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24413-67:
(7*2)+(6*4)+(5*4)+(4*1)+(3*3)+(2*6)+(1*7)=90
90 % 10 = 0
So 24413-67-0 is a valid CAS Registry Number.

24413-67-0SDS

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 1-N,4-N-bis(4-methoxyphenyl)benzene-1,4-diamine

1.2 Other means of identification

Product number -
Other names N,N'-di(4-anisyl)-1,4-benzenediamine

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:24413-67-0 SDS

24413-67-0Relevant articles and documents

Synthesis and characterization of novel electrochromic poly(amide-imide)s with N,N′-di(4-methoxyphenyl)-N,N′-diphenyl-p-phenylenediamine units

Hsiao, Sheng-Huei,Teng, Chia-Yin,Kung, Yu-Ruei

, p. 93591 - 93606 (2015/11/17)

We developed a new efficient procedure for the synthesis of a bistriphenylamine diamine monomer, N,N′-bis(4-aminophenyl)-N,N′-bis(4-methoxyphenyl)-1,4-phenylenediamine (3). A new dicarboxylic acid monomer bearing two built-in imide rings, namely N,N′-bis(

Preparation and characterization of N-Anisyl-substituted Hexaaza[1 6]paracyclophane

Ito, Akihiro,Yokoyama, Yuichiro,Aihara, Ryosuke,Fukui, Koji,Eguchi, Shoko,Shizu, Katsuyuki,Sato, Tohru,Tanaka, Kazuyoshi

supporting information; experimental part, p. 8205 - 8208 (2011/02/23)

Localized or delocalized? For the first time, a cyclic oligoaniline, hexaaza[16]paracyclophane, has been prepared (see picture; carbon: gray; nitrogen: blue; hydrogen: light gray). The macrocycle exhibits a high electron-donating ability, and furthermore, the spin of the corresponding radical cation was delocalized over the macrocyclic molecular backbone.

COMPOUNDS AND METHODS FOR TREATING PROTEIN FOLDING DISORDERS

-

Page/Page column 125-126, (2008/12/05)

The invention is directed to compounds and methods for treating protein folder disorders. In certain embodiments the invention provides compounds and methods for treating neurodegenerative diseases such as Alzheimer's disease, tauopathy, cerebral amyloid angiopathy, Lewy body disease, dementia, Huntington's disease and prion-based spongiform encelopathy. The invention further provides compounds, methods and pharmaceutical compositions for inhibiting tau protein, Aβ protein or α-synuclein protein aggregation.

Synthesis and alkylation of indolo[3,2-b]carbazoles

Yudina, Larisa N.,Bergman, Jan

, p. 1265 - 1275 (2007/10/03)

Double Fischer cyclisation was used to prepare indolo[3,2-b]carbazole and its 2,8-di-OMe, OH, Br and F-derivatives. N-monosubstituted derivatives of indolo[3,2-b]carbazole (methyl, hydroxymethyl, dimethylaminoethyl) were obtained starting from 5,11-di-Boc

Tetraazacyclophanes by palladium-catalyzed aromatic amination. Geometrically defined, stable, high-spin diradicals

Hauck, Sheila I.,Lakshmi,Hartwig, John F.

, p. 2057 - 2060 (2008/02/10)

matrix presented R = R′ =p-Me R = R′ = m-OMe R = R′ = p-OMe R = CO2t-Bu, R′ = p-OMe R = R′ = CO2t-Bu Neutral tetraazacyclophanes were prepared in a one-step palladium-catalyzed amination reaction. Simple oxidation of these materials

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