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17422-56-9

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17422-56-9 Usage

General Description

Diethyl 2-[(2-nitrophenyl)methylidene]propanedioate, also known as 2-nitrocinnamaldehyde diethyl acetal, is a chemical compound commonly used in organic synthesis. It is a yellow solid with a molecular formula C15H17NO5 and a molar mass of 287.30 g/mol. diethyl 2-[(2-nitrophenyl)methylidene]propanedioate is known for its aromatic and aliphatic properties, making it useful in the production of various aromatic and aliphatic derivatives. It is often used as a reagent in organic reactions and is also utilized in the manufacturing of pharmaceuticals, dyes, and agrochemicals. Overall, diethyl 2-[(2-nitrophenyl)methylidene]propanedioate plays a significant role in the advancement of chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17422-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,2 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17422-56:
(7*1)+(6*7)+(5*4)+(4*2)+(3*2)+(2*5)+(1*6)=99
99 % 10 = 9
So 17422-56-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO6/c1-3-20-13(16)11(14(17)21-4-2)9-10-7-5-6-8-12(10)15(18)19/h5-9H,3-4H2,1-2H3

17422-56-9SDS

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 diethyl 2-[(2-nitrophenyl)methylidene]propanedioate

1.2 Other means of identification

Product number -
Other names diethylmalonate,2-NO2 benzal

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:17422-56-9 SDS

17422-56-9Relevant articles and documents

Discovery of the Bruton's Tyrosine Kinase Inhibitor Clinical Candidate TAK-020 (S)-5-(1-((1-Acryloylpyrrolidin-3-yl)oxy)isoquinolin-3-yl)-2,4-dihydro-3 H-1,2,4-triazol-3-one, by Fragment-Based Drug Design

Sabat, Mark,Dougan, Douglas R.,Knight, Beverly,Lawson, J. David,Scorah, Nicholas,Smith, Christopher R.,Taylor, Ewan R.,Vu, Phong,Wyrick, Corey,Wang, Haixia,Balakrishna, Deepika,Hixon, Mark,Madakamutil, Loui,McConn, Donavon

supporting information, p. 12893 - 12902 (2021/09/13)

This publication details the successful use of FBDD (fragment-based drug discovery) principles in the invention of a novel covalent Bruton's tyrosine kinase inhibitor, which ultimately became the Takeda Pharmaceuticals clinical candidate TAK-020. Describe

Solvent-Free FeCl3-Assisted Electrophilic Fluorine-Catalyzed Knoevenagel Condensation to Yield α,β-Unsaturated Dicarbonyl Compounds and Coumarins

Yang, Lu,Zhu, Jiang,Xie, Fukai,Peng, Xiaoshi,Lin, Bin,Liu, Yongxiang,Cheng, Maosheng

, p. 1053 - 1060 (2019/09/06)

A highly environmentally friendly procedure was developed for the Knoevenagel condensation of aromatic aldehydes with diethyl malonate in the presence of FeCl3 and N-fluorobenzenesulfonimide as a source of electrophilic fluorine under solvent-free conditions. The scope of the reaction was explored using commercially available substrates. The reaction with substituted salicylaldehydes afforded the corresponding coumarin derivatives which attract interest due to their potential medicinal importance.

Visible-Light-Driven Intermolecular [2+2] Cycloadditions between Coumarin-3-Carboxylates and Acrylamide Analogs

Liu, Qiang,Zhu, Fu-Ping,Jin, Xiao-Ling,Wang, Xiao-Ju,Chen, Han,Wu, Li-Zhu

supporting information, p. 10326 - 10329 (2015/07/07)

This paper reports a room temperature visible-light-driven protocol for the intermolecular [2+2] cycloadditions between coumarin-3-carboxylates and acrylamides analogs by an energy-transfer process. Using an iridium complex FIrPic as a photosensitizer and a 3W blue LED as a light source, an array of cyclobutabenzocypyranones were prepared in moderate to excellent yields.

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