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2-Butenedioic acid, 2,3-diphenyl-, diethyl ester, (Z)-, also known as (Z)-Diethyl 2,3-diphenylmaleate, is an organic compound with the chemical formula C18H16O4. It is a colorless to pale yellow liquid with a molecular weight of 300.31 g/mol. 2-Butenedioic acid, 2,3-diphenyl-, diethyl ester, (Z)- is characterized by its maleic anhydride structure, featuring two phenyl groups attached to the 2 and 3 positions, and two ester groups derived from ethanol. It is synthesized by reacting diphenylmaleic anhydride with ethanol in the presence of a catalyst. (Z)-Diethyl 2,3-diphenylmaleate is used as a chemical intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed in the synthesis of polymers and resins. Due to its reactivity, it is essential to handle 2-Butenedioic acid, 2,3-diphenyl-, diethyl ester, (Z)- with care, following proper safety protocols.

5635-39-2

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5635-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5635-39-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5635-39:
(6*5)+(5*6)+(4*3)+(3*5)+(2*3)+(1*9)=102
102 % 10 = 2
So 5635-39-2 is a valid CAS Registry Number.

5635-39-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl (Z)-2,3-diphenylmaleate

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5635-39-2 SDS

5635-39-2Relevant academic research and scientific papers

Unified Synthesis of Azepines by Visible-Light-Mediated Dearomative Ring Expansion of Aromatic N-Ylides

Mailloux, Matthew J.,Fleming, Gabrielle S.,Kumta, Shruti S.,Beeler, Aaron B.

, p. 525 - 529 (2021/01/26)

Herein, we report a unified approach to azepines by dearomative photochemical rearrangement of aromatic N-ylides. Deprotonation of quaternary aromatic salts with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or N,N,N′,N'-tetramethylquanidine (TMG) under visible light irradiation provides mono- and polycyclic azepines in yields up to 98%. This ring-expansion presents a new mode of access to functionalized azepines from N-heteroarenes using two straightforward steps and simple starting materials.

Copper(I)-catalyzed aerobic oxidation of α-diazoesters

Xu, Changming,Bai, Lei,Wang, Yongchang

supporting information, p. 12579 - 12584 (2020/11/09)

A practical Cu-catalyzed oxidation of α-diazoesters to α-ketoesters using molecular oxygen as an oxidant has been developed. Both electron-poor and electron-rich aryl α-diazoesters are suitable substrates and provide the α-ketoesters in good yields. In this oxidative system, α-diazo-β-ketoesters are also compatible as substrates but unexpectedly furnish α-ketoesters via C-C bond cleavage, rather than the vicinal tricarbonyl products.

Regio- and stereoselective route to tetrasubstituted olefins by the palladium-catalyzed three-component coupling of aryl iodides, internal alkynes, and arylboronic acids

Zhou, Chengxiang,Larock, Richard C.

, p. 3765 - 3777 (2007/10/03)

The Pd-catalyzed three-component coupling of readily available aryl iodides, internal alkynes, and arylboronic acids provides a convenient, one-step, regio- and stereoselective route to tetrasubstituted olefins in good to excellent yields, although electron-poor aryl iodides and dialkylalkynes normally afford only low yields under our standard reaction conditions. The proper combination of substrates and reaction conditions is important for high yields. The presence of water generally substantially increases the yields of the desired tetrasubstituted olefins. The reaction involves cis-addition of the aryl group from the aryl iodide to the less hindered or more electron-rich end of the alkyne, while the aryl group from the arylboronic acid adds to the other end. A modified, room-temperature procedure has also been successfully developed, which works very well for some substrates. Tamoxifen and its derivatives are synthesized in a concise, regio- and stereoselective manner by applying our synthetic protocol.

A new access to diarylmaleic anhydrides

Beccalli, Egle M.,Gelmi, Maria Luisa,Marchesini, Alessandro

, p. 1421 - 1426 (2007/10/03)

A new three-step synthesis of diarylmaleic anhydrides 6, starting from 3-aryl-2-hydroxybut-2-enedioates 2, is reported.

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