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The chemical compound "3-[(5E)-5-(2-methoxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]-N-(5-methyl-1,3,4-thiadiazol-2-yl)propanamide" is a complex organic molecule with a molecular formula of C18H15N3O4S3. It features a 1,3-thiazolidin-3-yl core, which is a heterocyclic ring system containing sulfur and nitrogen atoms. The compound has a 5-methyl-1,3,4-thiadiazol-2-yl group attached to the nitrogen atom of the propanamide chain, which extends from the 3-position of the thiazolidinyl ring. Additionally, the molecule includes a 2-methoxybenzylidene moiety, which is a benzylidene group with a methoxy substituent, and a 4-oxo-2-thioxo group, indicating the presence of a carbonyl and a thioxo (sulfur analog of a carbonyl) functional groups. 3-[(5E)-5-(2-methoxybenzylidene)-4-oxo-2-thioxo-1,3-thiazolidin-3-yl]-N-(5-methyl-1,3,4-thiadiazol-2-yl)propanamide is characterized by its unique structure and potential applications in various fields, such as pharmaceuticals or materials science, due to its diverse functional groups and complex structure.

5526-61-4

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5526-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5526-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5526-61:
(6*5)+(5*5)+(4*2)+(3*6)+(2*6)+(1*1)=94
94 % 10 = 4
So 5526-61-4 is a valid CAS Registry Number.

5526-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-acetylphenyl)-3-(methoxymethyl)-1-benzofuran-2-carboxamide

1.2 Other means of identification

Product number -
Other names N-(3-acetylphenyl)-3-(methoxymethyl)benzofuran-2-carboxamide

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:5526-61-4 SDS

5526-61-4Relevant academic research and scientific papers

Development of Potent Type i Protein Arginine Methyltransferase (PRMT) Inhibitors of Leukemia Cell Proliferation

Wang, Chen,Jiang, Hao,Jin, Jia,Xie, Yiqian,Chen, Zhifeng,Zhang, Hao,Lian, Fulin,Liu, Yu-Chih,Zhang, Chenhua,Ding, Hong,Chen, Shijie,Zhang, Naixia,Zhang, Yuanyuan,Jiang, Hualiang,Chen, Kaixian,Ye, Fei,Yao, Zhiyi,Luo, Cheng

, p. 8888 - 8905 (2017/11/14)

Protein Arginine Methyltransferases (PRMTs) are crucial players in diverse biological processes, and dysregulation of PRMTs has been linked to various human diseases, especially cancer. Therefore, small molecules targeting PRMTs have profound impact for both academic functional studies and clinical disease treatment. Here, we report the discovery of N1-(2-((2-chlorophenyl)thio)benzyl)-N1-methylethane-1,2-diamine (28d, DCPR049-12), a highly potent inhibitor of type I PRMTs that has good selectivity against a panel of other methyltransferases. Compound 28d effectively inhibits cell proliferation in several leukemia cell lines and reduces the cellular asymmetric arginine dimethylation levels. Serving as an effective inhibitor, 28d demonstrates the mechanism of cell killing in both cell cycle arrest and apoptotic effect as well as downregulation of the pivotal mixed lineage leukemia (MLL) fusion target genes such as HOXA9 and MEIS1, which reflects the critical roles of type I PRMTs in MLL leukemia. These studies present 28d as a valuable inhibitor to investigate the role of type I PRMTs in cancer and other diseases.

Synthesis of naphtho[2,3-b]-and naphtho[1,2-b]-fused thieno[2,3-d][1] benzoxepins and thieno[2,3-d][1]-benzothiepins

Landek, Ivana Ozimec,Pesic, Dijana,Trojko, Rudolf,Bogdanovic, Maja Devcic,Mercep, Mladen,Mesic, Milan

experimental part, p. 2269 - 2290 (2011/03/23)

Synthesis of four novel classes of structurally related fused hetero-pentacyclic compounds, naphtho[2,3-b]thieno[2,3-d][1]benzothiepins (Ia), naphtho[1,2-b]thieno[2,3-d][1]benzothiepins (IIa), naphtho[2,3-b]thieno-[2,3-d] [1]benzoxepins (Ib, c) and naphth

1- OR 3-THIA-BENZONAPHTHOAZULENES AS INHIBITORS OF TUMOUR NECROSIS FACTOR PRODUCTION AND INTERMEDIATES FOR THE PREPARATION THEREOF

-

Page/Page column 35-36, (2008/06/13)

The present invention relates to 1- or 3-thiabenzonaphthoazulene derivatives to their pharmacologically acceptable salts and solvates, to processes and intermediates for the preparation thereof as well as to their antiinflammatory effects, especially to t

The Synthesis of Some Derivatives of Benzonaphtothiepin-12-one

Flores, Maria Celia,Beller, Nicholas R.,Castrillon, Jose

, p. 1737 - 1739 (2007/10/02)

The preparations of benzonaphthothiepin-12-one, its 6-methyl and 6-methoxy derivatives and their corresponding sulfoxides and sulfones are described.They involve the coupling of suitable halogen naphthyl derivatives with thiophenoxides with the

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