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2-Butenedinitrile, 2,3-bis(4-methylphenyl)-, also known as 2,3-bis(4-methylphenyl)-2-butenedinitrile or 4,4'-(2-butenedinitrile)dianiline, is an organic compound with the chemical formula C16H14N2. It is a yellow crystalline solid that is soluble in organic solvents. 2-Butenedinitrile, 2,3-bis(4-methylphenyl)- is primarily used as a monomer in the production of high-performance polymers, such as polyimides and polyamides, which are known for their excellent thermal stability, mechanical properties, and chemical resistance. These polymers find applications in various industries, including aerospace, electronics, and automotive, where high-temperature resistance and durability are required. The compound is also used in the synthesis of other specialty chemicals and as a research chemical in the field of organic chemistry.

4941-71-3

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4941-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4941-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4941-71:
(6*4)+(5*9)+(4*4)+(3*1)+(2*7)+(1*1)=103
103 % 10 = 3
So 4941-71-3 is a valid CAS Registry Number.

4941-71-3Relevant academic research and scientific papers

Intermolecular interactions-photophysical properties relationships in phenanthrene-9,10-dicarbonitrile assemblies

Afanasenko, Anastasiia M.,Novikov, Alexander S.,Chulkova, Tatiana G.,Grigoriev, Yakov M.,Kolesnikov, Ilya E.,Selivanov, Stanislav I.,Starova, Galina L.,Zolotarev, Andrey A.,Vereshchagin, Anatoly N.,Elinson, Michail N.

, (2019/09/09)

Phenanthrene-9,10-dicarbonitriles show various luminescence behaviour in solution and in the solid state. Aggregation patterns of phenanthrene-9,10-dicarbonitriles govern their luminescent properties in the solid state. Single crystal structures of phenan

A two-cyano diaryl ethylene synthetic method of the compound (by machine translation)

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Paragraph 0039-0042, (2018/07/10)

The present invention discloses a two-cyano diaryl ethylene compound synthetic methods, the method in the air atmosphere, in order to replace the benzyl cyanide as raw materials, to Ru/C, K2 CO3 As the catalyst, in ortho-dichlorobenz

Structures and photophysical properties of 3,4-diaryl-1H-pyrrol-2,5-diimines and 2,3-diarylmaleimides

Afanasenko, Anastasiia M.,Boyarskaya, Dina V.,Boyarskaya, Irina A.,Chulkova, Tatiana G.,Grigoriev, Yakov M.,Kolesnikov, Ilya E.,Avdontceva, Margarita S.,Panikorovskii, Taras L.,Panin, Andrej I.,Vereshchagin, Anatoly N.,Elinson, Michail N.

, p. 554 - 561 (2017/06/20)

Structural features of 3,4-diaryl-1H-pyrrol-2,5-diimines and their derivatives have been studied by molecular spectroscopy techniques, single-crystal X-ray diffraction, and DFT calculations. According to the theoretical calculations, the diimino tautomeri

Diarylmaleimide-based branched oligomers: Strong full-color emission in both solution and solid films

Wang, Jingwei,Zheng, Rong,Chen, Huan,Yao, Huimei,Yan, Liyu,Wei, Jie,Lin, Zhenghuan,Ling, Qidan

supporting information, p. 130 - 139 (2017/12/27)

Maleimide and benzene are employed as a dendron and a core, respectively, to construct two series of non-conjugate branched oligomers (B3G1 and B1G2) based on diarylmaleimide fluorophores by an alkylation reaction. Surface aryl groups are changed to tune

Emitting color adjustable dendritic macromolecular fluorescent material and preparation method thereof

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Page/Page column 12, (2018/01/14)

The invention relates to an emitting color adjustable dendritic macromolecular fluorescent material and a preparation method of the fluorescent material. A benzene ring serves as a nucleus; 3,4-diaryl substituted maleimide serves as a branch; two-direction, three-direction and four-direction initiated first-generation dendritic macromolecules (B2G1, B3G1 and B4G1), and one-direction initiated second-generation dendritic macromolecules (B1G2) are constructed by an alkylation reaction; an emitting color of the dendritic fluorescent material is effectively adjusted by changing a push-pull electronic effect of a peripheral group (S); and full-color light emitting from blue to red is achieved. The dendritic fluorescent material has the advantages of adjustable emitting color, high solid fluorescence quantum efficiency and the like; the fluorescent material has good solubility in various solvents such as chloroform, methylbenzene, tetrahydrofuran and chlorobenzene; and a high-quality film can be obtained by methods of spin-coating or ink-jet printing and the like. Therefore, the material has very wide application prospects in organic electroluminescence, organic laser and full-color display.

Labeled compound and detection method using the same

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Page/Page column 20, (2011/12/12)

A labeled compound is so designed that an aromatic tertiary amine compound is bondable with a biomolecule. One of S1 and S2 contains a group bound with a molecular chain 10 (e.g. an oligonucleotide) capable of binding with a biomolec

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