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"5-[2-(benzyloxy)-5-chlorobenzylidene]-3-(prop-2-en-1-yl)-2-thioxo-1,3-thiazolidin-4-one" is a complex organic compound characterized by a 1,3-thiazolidin-4-one core structure. This molecule features a 5-chlorobenzylidene group attached to the thiazolidinone ring through a benzyloxy linker, indicating the presence of a benzyl group connected to an oxygen atom that bridges to the aromatic ring. Additionally, a prop-2-en-1-yl group is attached to the 3-position of the thiazolidinone ring, introducing a double bond and an alkene functional group. The 2-position of the thiazolidinone ring is occupied by a thioxo group, which is a sulfur-oxygen double bond, contributing to the compound's reactivity and potential applications in chemical research and pharmaceutical development. 5-[2-(benzyloxy)-5-chlorobenzylidene]-3-(prop-2-en-1-yl)-2-thioxo-1,3-thiazolidin-4-one's structure suggests it may have unique chemical properties and could be of interest in the synthesis of various pharmaceuticals or as a precursor in organic synthesis.

4355-42-4

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4355-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4355-42-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4355-42:
(6*4)+(5*3)+(4*5)+(3*5)+(2*4)+(1*2)=84
84 % 10 = 4
So 4355-42-4 is a valid CAS Registry Number.

4355-42-4SDS

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 5-[(5-chloro-2-phenylmethoxyphenyl)methylidene]-3-prop-2-enyl-2-sulfanylidene-1,3-thiazolidin-4-one

1.2 Other means of identification

Product number -
Other names (5Z)-5-[2-(benzyloxy)-5-chlorobenzylidene]-3-(prop-2-en-1-yl)-2-thioxo-1,3-thiazolidin-4-one

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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More Details:4355-42-4 SDS

4355-42-4Relevant academic research and scientific papers

Cobalt-catalyzed C[sbnd]H activation/C[sbnd]O formation: Synthesis of benzofuranones

Hajipour, Abdol R.,Khorsandi, Zahra

, (2019/11/26)

Herein, C[sbnd]H activation/C[sbnd]O formation reaction using novel cobalt catalytic system is reported. This reaction was given benzofuranones in moderate to excellent yields at room-temperature under air reaction conditions. The introduced strategy is efficient and low-cost method to synthesized benzofuranones from α,α-disubstitution acetic acid.

Palladium-catalyzed bisarylation of 3-alkylbenzofurans to 3-arylalkyl-2-arylbenzofurans on water: Tandem C(sp3)-H and C(sp2)-H activation reactions of 3-alkylbenzofurans

Cho, Beom Shin,Chung, Young Keun

supporting information, p. 14543 - 14546 (2015/09/28)

A protocol involving facile sequential C(sp3)-H and C(sp2)-H activation reactions of 3-alkylbenzofurans catalyzed by Pd(OAc)2 in the presence of pivalic acid, silver salt, and tricyclohexylphosphine 'on water' was developed. Aryl iodides were used as substrates in a tandem bisarylation reaction to generate 3-arylalkyl-2-arylbenzofurans in moderate to high yields at room temperature. The reaction revealed in this study is a rare example of consecutive C(sp3)-H and C(sp2)-H bond activation under mild reaction conditions.

Imidazole derivatives as accelerators for ruthenium-catalyzed hydroesterification and hydrocarbamoylation of alkenes: Extensive ligand screening and mechanistic study

Konishi, Hideyuki,Muto, Takashi,Ueda, Tsuyoshi,Yamada, Yayoi,Yamaguchi, Miyuki,Manabe, Kei

, p. 836 - 845 (2015/03/14)

Imidazole derivatives are effective ligands for promoting the [Ru3(CO)12]-catalyzed hydroesterification of alkenes using formates. Extensive ligand screening was performed to identify 2-hydroxymethylated imidazole as the optimal ligand. Neither carbon monoxide gas nor a directing group was required, and the reaction also showed a wide substrate generality. The Ru-imidazole catalyst system also promoted intramolecular hydrocarbamoylation to afford lactams. A Ru-imidazole complex was unambiguously analyzed by X-ray crystallography, and it had a trinuclear structure derived from one [Ru3(CO)12] and two ligands. This complex was also successfully used for hydroesterification. The mechanism was examined in detail by using D- and 13C-labeled formates, indicating that the hydroesterification reaction proceeds by a decarbonylation-recarbonylation pathway. Effective imidazole assistant: [Ru3(CO)12]-catalyzed hydroesterification of alkenes by using formates is drastically accelerated by imidazole derivatives and exhibits a broad substrate scope for both alkenes and formates. The Ru-imidazole complex also catalyzes the intramolecular hydrocarbamoylation of alkenes.

Direct lactonization of 2-arylacetic acids through Pd(II)-catalyzed C-H activation/C-O formation

Yang, Mingyu,Jiang, Xingyu,Shi, Wen-Juan,Zhu, Qi-Lei,Shi, Zhang-Jie

, p. 690 - 693 (2013/04/10)

Palladium-catalyzed direct lactonization of 2-arylacetic acids through a reaction sequence that includes C-H activation/C-O formation is reported. This method provides a concise and efficient pathway to synthesize fully functionalized benzofuranone derivatives, which are highly relevant to bioactive natural and synthetic products.

Remarkable improvement achieved by imidazole derivatives in ruthenium-catalyzed hydroesterification of alkenes using formates

Konishi, Hideyuki,Muto, Takashi,Manabe, Kei,Ueda, Tsuyoshi

supporting information, p. 4722 - 4725,4 (2012/12/12)

Imidazole derivatives are revealed to be effective ligands in the Ru-catalyzed hydroesterification of alkenes using formates, affording one-carbonelongated esters in high yields. Further, intramolecular hydroesterification was successfully performed to give lactones for the first time. Imidazole derivatives can contribute to promote the reaction as well as to suppress the undesired decarbonylation of formate. Toxic CO gas, a directing group, and large excess alkenes are not required.

Dimethyldioxirane epoxidation of 3-phenyl-substituted benzofurans: A reversible valence isomerization between benzofuran epoxides and quinone methides

Adam,Peters,Sauter

, p. 111 - 119 (2007/10/02)

Low-temperature oxidation of the phenyl-substituted benzofurans 1 by dimethyldioxirane afforded the rather labile benzofuran epoxides 2, which are in equilibrium with their equally labile quinone methides 3 through valence isomerization. This reversible v

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