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24115-28-4

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24115-28-4 Usage

Description

[methyl(phenyl)amino]methylidenepropanedinitrile, commonly referred to as MAPD, is a complex organic molecule with the molecular formula C11H10N2. It features a propanedinitrile core and a methyl(phenyl)amino substituent, which contributes to its unique structure and reactivity. This versatile compound is widely utilized in the field of organic synthesis and materials science, making it a valuable asset for creating diverse and complex molecules.

Uses

Used in Pharmaceutical Industry:
MAPD is used as a building block and intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, MAPD serves as a crucial intermediate for the production of various agrochemicals, such as pesticides and fertilizers. Its role in this industry is essential for the development of effective and environmentally friendly solutions for agricultural needs.
Used in Organic Synthesis:
As a highly reactive compound, MAPD is employed in organic synthesis to create a wide range of complex molecules. Its versatility makes it an indispensable tool in the development of new materials and functional organic compounds.
Used in Materials Science:
MAPD's potential utility extends to the field of materials science, where it is explored for its ability to contribute to the development of innovative materials with unique properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 24115-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,1 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24115-28:
(7*2)+(6*4)+(5*1)+(4*1)+(3*5)+(2*2)+(1*8)=74
74 % 10 = 4
So 24115-28-4 is a valid CAS Registry Number.

24115-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(N-methylanilino)methylidene]propanedinitrile

1.2 Other means of identification

Product number -
Other names <N-Methyl-anilinomethylen>-malonsaeure-dinitril

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:24115-28-4 SDS

24115-28-4Downstream Products

24115-28-4Relevant articles and documents

Extremely Reactive C=C Double Bonds, VI. - Tris(methylphenylamino)methane - The Chemistry of Orthoamides

Schoenberg, Alexander,Singer, Erich,Stephan, Werner

, p. 1581 - 1588 (2007/10/02)

Reactions of the title compound 2 with sulfur, selenium, thiophenol, malononitrile, 1,3-indanedione, fluorenone hydrazone, phenylmagnesium bromide, bromine, thioacetic acid, N,N'-diphenylurea, oxalyl chloride, 9,9-dichloroxanthene, phenyl isocyanate, and stilbene dibromide are described and the mechanisms are discussed.The catalytic influence of 2 on the decomposition of 9-diazofluorene in xylene and mesitylene is discussed.

Cyanoacrylates. Herbicidial and Photosynthetic Inhibitory Activity

Huppatz, John L.,Phillips, John N.,Rattigan, Barbara M.

, p. 2769 - 2774 (2007/10/02)

Various alkyl 3-ohenylamino-2-cyano- and 2-ethoxycarbonylacrylates and 3-phenylamino-2-cyanoacrylonitriles were synthesized and assayed as inhibitors of the Hill reaction in isolated pea chloroplast suspensions and as pre- and post-emergent herbicides on mustard and barnyard grass.Many of the compounds were potent Hill reaction inhibitors and several showed significant herbicidial activity.

On the condensation of acid amides with active methylene compounds and the preparation of new thiazole derivatives.

EIDEN

, p. 516 - 523 (2007/10/05)

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