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(E)-2,4-dimethoxycinnamic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42174-73-2

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42174-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42174-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,1,7 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42174-73:
(7*4)+(6*2)+(5*1)+(4*7)+(3*4)+(2*7)+(1*3)=102
102 % 10 = 2
So 42174-73-2 is a valid CAS Registry Number.

42174-73-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2,4-dimethoxycinnamic acid ethyl ester

1.2 Other means of identification

Product number -
Other names ethyl 2,4-dimethoxycinnamate

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:42174-73-2 SDS

42174-73-2Relevant academic research and scientific papers

S,O-Ligand-Promoted Pd-Catalyzed C?H Olefination of Anisole Derivatives

Fernández-Ibá?ez, M. ángeles,Jia, Wen-Liang,Sukowski, Verena,van Borselen, Manuela,van Diest, Rianne

supporting information, p. 4132 - 4135 (2021/08/24)

The C?H olefination of substituted anisole derivatives by a Pd/S,O-ligand catalyst is reported. The reaction proceeds under mild conditions with a broad range of substituted aryl ethers bearing both electron donating and withdrawing substituents at ortho,

Synthesis of Bidentate Nitrogen Ligands by Rh-Catalyzed C-H Annulation and Their Application to Pd-Catalyzed Aerobic C-H Alkenylation

Kim, Hyun Tae,Kang, Eunsu,Kim, Minkyu,Joo, Jung Min

supporting information, p. 3657 - 3662 (2021/05/10)

A new class of bidentate ligands was prepared by a modular approach involving Rh-catalyzed C-H annulation reactions. The resulting conformationally constrained ligands enabled the Pd-catalyzed C-H alkenylation at electron-rich and sterically less hindered positions of electron-rich arenes while promoting the facile oxidation of Pd(0) intermediates by oxygen. This newly introduced ligand class is complementary to the ligands developed for Pd-catalyzed oxidative reactions and may find broad application in transition-metal-catalyzed reactions.

Synthesis of methoxylated goniothalamin, aza-goniothalamin and γ-pyrones and their in vitro evaluation against human cancer cells

Barcelos, Rosimeire Coura,Pastre, Julio Cezar,Caixeta, Vanessa,Vendramini-Costa, Débora Barbosa,De Carvalho, Jo?o Ernesto,Pilli, Ronaldo Aloise

experimental part, p. 3635 - 3651 (2012/07/27)

The present work describes the preparation of three novel series of compounds based on the structure of goniothalamin, a natural styryl lactone which has been found to display cytotoxic and antiproliferative activities against a variety of cancer cell lines. A focused library of 29 novel goniothalamin analogues was prepared and evaluated against seven human cancer cell lines. While the γ-pyrones and the aza-goniothalamin analogues were less potent than the lead compound, 2,4-dimethoxy analogue 88 has shown to be more potent in vitro than goniothalamin against all cancer cell lines evaluated. Furthermore, it was more potent than doxorubicin against NCI-ADR/RES, OVCAR-03 and HT-29 while being less toxic to human keratinocytes (HaCat). The 3,5-dimethoxy analogue 90 and 2,4,5-trimethoxy analogue 92 also displayed promising antiproliferative activity when compared to goniothalamin (1). These results provide new elements for the design and synthesis of novel representatives of this family of natural compounds.

Synthesis of C-Alkyl Calixarenes. 3. Acid-Catalyzed Rearrangement of 2,6-Dimethoxycinnamate Prior to Tetramerization to Calixarenes

Botta, Bruno,Delle Monache, Giuliano,De Rosa, Maria,Carbonetti, Angela,Gacs-Baitz, Eszter,et al.

, p. 3657 - 3662 (2007/10/02)

In our continuing studies concerning the versatility of the acid-catalyzed conversion of cinnamates to calixresorcinarenes, we have demonstrated that 2,6-dimethoxycinnamic acid ethyl ester 3 undergoes an interesting rearrangement to afford the same cal

Acid-labile anchor groups for the synthesis of peptide amides by a solid-phase method

-

, (2008/06/13)

The invention relates to new compounds of the formula STR1 in which R1 denotes (C1 -C8)-alkyl, R2 denotes an amino acid residue which is protected with a urethane protective group which can be eliminated with weak acid or base, or denotes an amino protective group which can be eliminated with weak acid or base, R3 denotes hydrogen or (C1 -C4)-alkyl, and Y1 -Y9 denote identical or different radicals hydrogen, (C1 -C4)-alkyl, (C1 -C4)-alkoxy or --O--(CH2)n --COOH (with n=1 to 6), with one of these radicals being --O--(CH2)n --COOH, or Y1, Y2 and Y5 -Y9 denote identical or different radicals hydrogen, (C1 -C4)-alkyl or (C1 -C4)-alkoxy, Y3 denotes hydrogen or (C1 -C8)-alkoxy and Y4 denotes --(CH2)n --COOH or --NH--CO--(CH2)n --COOH (with n=1 to 6). Processes for the preparation thereof and the synthesis of peptide amides by a solid-phase method using these new compounds (spacers) are described.

REACTION OF BENZYLIDENEBENZYLAMINE WITH CINNAMIC ACID DERIVATIVES UNDER CONDITIONS OF PHASE-TRANSFER CATALYSIS. I. SYNTHESIS OF β-ARYL-γ-PHENYL-γ-AMINOBUTYRIC ACIDS AND THEIR DERIVATIVES

Potapov, V. M.,Gracheva, R. A.,Sivov, N. A.,Savina, S. A.,Sivova, L. A.

, p. 1694 - 1699 (2007/10/02)

The reaction of benzylidenebenzylamine with the esters of substituted cinnamic acids under the conditions of phase-transfer catalysis gives high yields of β-aryl-γ-phenyl-γ-aminobutyric acids and their derivatives (hydrochlorides, 4-aryl-5-phenyl-2-pyrrolidones).

Substituent Effects in the Reaction of t-Butylmagnesium Chloride with Substituted Ethyl Cinnamates. A Correlation with 13C NMR Chemical Shifts

Jalander, Lars

, p. 419 - 428 (2007/10/02)

The reaction of t-butylmagnesium chloride with some substituted ethyl (E)-cinnamates gave mainly 1,3-, 1,4-, 1,2- and 1,4-addition products and minor amounts of 1,2- and 1,3-addition products.The relative amounts of 1,3-addition products has been shown to correlate with 13C NMR chemical shifts of C-α of the ethyl cinnamates.The correlation indicates that the regio selectivity of the reactions is to a great extent dependent of polar effects and that the t-butyl radical has a nucleophilic character.

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