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(3-hydroxybenzo[b]thiophen-2-yl)(p-tolyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77946-35-1

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77946-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77946-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,4 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77946-35:
(7*7)+(6*7)+(5*9)+(4*4)+(3*6)+(2*3)+(1*5)=181
181 % 10 = 1
So 77946-35-1 is a valid CAS Registry Number.

77946-35-1Downstream Products

77946-35-1Relevant academic research and scientific papers

Synthesis of Double-Bond-Substituted Hemithioindigo Photoswitches

Gerwien, Aaron,Reinhardt, Till,Mayer, Peter,Dube, Henry

, p. 232 - 235 (2018)

A very short, high yielding, and convergent synthesis with broad substrate scope, enabling access to a very diverse range of hemithioindigos with 4-fold substituted double-bonds, is presented. With this method, carbon as well as nitrogen, oxygen, or sulfur based substituents can easily be introduced, delivering a wide array of novel structural motifs. Irradiation studies with visible light demonstrate proficient photoswitching properties of these chromophores at wavelengths up to 625 nm.

Benzo[b]tiophen-3-ol derivatives as effective inhibitors of human monoamine oxidase: design, synthesis, and biological activity

Guglielmi, Paolo,Secci, Daniela,Petzer, Anél,Bagetta, Donatella,Chimenti, Paola,Rotondi, Giulia,Ferrante, Claudio,Recinella, Lucia,Leone, Sheila,Alcaro, Stefano,Zengin, Gokhan,Petzer, Jacobus P.,Ortuso, Francesco,Carradori, Simone

, p. 1511 - 1525 (2019/08/26)

A series of benzo[b]thiophen-3-ols were synthesised and investigated as potential human monoamine oxidase (hMAO) inhibitors in vitro as well as ex vivo in rat cortex synaptosomes by means of evaluation of 3,4-dihydroxyphenylacetic acid/dopamine (DOPAC/DA)

Use of Phenacyl Thiosalicylates for the Preparation of 3-Hydroxybenzo[ b ]thiophene Derivatives

Trapani, Patricia,Kvapil, Lubomír,Hradil, Pavel,Soural, Miroslav

supporting information, p. 810 - 814 (2018/02/16)

In this work, we attempted to synthesize thioflavonols using rearrangement of phenacyl thiosalicylates prepared by two different approaches and subjected to cyclization under acidic conditions. Contrary to our expectations, the isolated products were iden

Iron-ligand coordination in tandem radical cyclizations: Synthesis of benzo[b]thiophenes by a one-pot reaction of iron 1,3-diketone complexes with 2-thiosalicylic acids

Chan, Sharon Lai-Fung,Low, Kam-Hung,Yang, Chen,Cheung, Samantha Hui-Fung,Che, Chi-Ming

supporting information; experimental part, p. 4709 - 4714 (2011/06/17)

Iron-the mediator: 1,3-Diketone ligands coordinated to iron undergo unprecedented tandem reactions with 2-thiosalicylic acids to give 2-substituted 3-hydroxylbenzo[b]thiophenes in up to 98 % yield. A similar reaction with 2-mercaptonicotinic acid gave a thieno[2,3-b]pyridine derivative in 72 % yield (see scheme). A mechanism involving redox transformation and tandem radical cyclization of the coordinated ligands is proposed. Copyright

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