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(E)-2-(4-(3-nitrophenyl)but-3-en-1-yl)isoindoline-1,3-dione is a complex organic compound characterized by its unique molecular structure. It features an isoindoline-1,3-dione core, which is a derivative of phthalimide, a well-known chemical used in various industrial applications. The compound is further distinguished by the presence of a 3-nitrophenyl group attached to a but-3-en-1-yl chain, which extends from the isoindoline core. The "E" configuration indicates the geometric isomerism of the double bond in the butenyl chain, suggesting a specific arrangement of the substituents around the double bond. (E)-2-(4-(3-nitrophenyl)but-3-en-1-yl)isoindoline-1,3-dione may be of interest in chemical research and development due to its potential applications in the synthesis of pharmaceuticals, dyes, or other specialty chemicals.

84812-15-7

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84812-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84812-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,1 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84812-15:
(7*8)+(6*4)+(5*8)+(4*1)+(3*2)+(2*1)+(1*5)=137
137 % 10 = 7
So 84812-15-7 is a valid CAS Registry Number.

84812-15-7Downstream Products

84812-15-7Relevant academic research and scientific papers

Benzazepine Dicarboxamide Compounds

-

, (2016/09/26)

This invention relates to novel benzazepine dicarboxamide compounds of the formula wherein R1 to R4 are as defined in the description and in the claims, as well as pharmaceutically acceptable salts thereof. These compounds are TLR agonists and may therefore be useful as medicaments for the treatment of diseases such as cancer, autoimmune diseases, inflammation, sepsis, allergy, asthma, graft rejection, graft-versus-host disease, immunodeficiencies, and infectious diseases.

Role of the Through-Space 2p-3d Overlap Effect in the Wittig Reaction

McEwen, William E.,Cooney, John V.

, p. 983 - 987 (2007/10/02)

Reactions of the ylide derived from triphenyl(3-phthalimidopropyl)phosphonium bromide with aromatic aldehydes have been reported to give exclusively the Z alkenes.On the basis of the Bestmann mechanism for the Wittig reaction, and also because of the fact that a 2,6-dimethoxyphenyl group enters into a strong through-space 2p-3d overlap interaction with an adjacent phosphonio group, we postulated that the reactions of the ylide derived from (2,6-dimethoxyphenyl)diphenyl(3-phthalimidopropyl)phosphonium bromide with aromatic aldehydes would give substantial ratios of E:Z alkenes.This proved to be the case.

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