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681161-44-4

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681161-44-4 Usage

General Description

3'-Hydroxybiphenyl-3-carboxamide is a chemical compound characterized by the presence of hydroxy, biphenyl, and carboxamide groups. Being a derivative of biphenyl, it falls under the category of organic compounds known as biphenyls and derivatives, which consists of compounds containing a biphenyl moiety, that is a structure made of two benzene rings linked together. This chemical compound is crucial in various chemical reactions and can act as an effective intermediate in organic synthesis. Its properties and behavior can vary based on many factors like temperature, pH, and its interaction with other chemical substances.

Check Digit Verification of cas no

The CAS Registry Mumber 681161-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,1,1,6 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 681161-44:
(8*6)+(7*8)+(6*1)+(5*1)+(4*6)+(3*1)+(2*4)+(1*4)=154
154 % 10 = 4
So 681161-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H11NO2/c14-13(16)11-5-1-3-9(7-11)10-4-2-6-12(15)8-10/h1-8,15H,(H2,14,16)

681161-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3'-Hydroxy-[1,1'-biphenyl]-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3-(3-hydroxyphenyl)benzamide

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:681161-44-4 SDS

681161-44-4Relevant articles and documents

Identification of bivalent ligands with melatonin receptor agonist and fatty acid amide hydrolase (FAAH) inhibitory activity that exhibit ocular hypotensive effect in the rabbit

Spadoni, Gilberto,Bedini, Annalida,Furiassi, Lucia,Mari, Michele,Mor, Marco,Scalvini, Laura,Lodola, Alessio,Ghidini, Andrea,Lucini, Valeria,Dugnani, Silvana,Scaglione, Francesco,Piomelli, Daniele,Jung, Kwang-Mook,Supuran, Claudiu T.,Lucarini, Laura,Durante, Mariaconcetta,Sgambellone, Silvia,Masini, Emanuela,Rivara, Silvia

, p. 7902 - 7916 (2018/09/18)

Activation of melatonin receptors and inhibition of fatty acid amide hydrolase (FAAH) have both shown potential benefits for the treatment of glaucoma. To exploit the combination of these biological activities in single therapeutic agents, we designed dua

As opioid receptor antagonists or inverse agonists of the novel compounds

-

Paragraph 0146-0149; 0151, (2016/10/08)

Novel compounds which are antagonists or inverse agonists at one or more of the opioid receptors, pharmaceutical compositions containing them, to processes for their preparation.

Applying a multitarget rational drug design strategy: The first set of modulators with potent and balanced activity toward dopamine D3 receptor and fatty acid amide hydrolase

De Simone, Alessio,Ruda, Gian Filippo,Albani, Clara,Tarozzo, Glauco,Bandiera, Tiziano,Piomelli, Daniele,Cavalli, Andrea,Bottegoni, Giovanni

supporting information, p. 4904 - 4907 (2014/05/06)

Combining computer-assisted drug design and synthetic efforts, we generated compounds with potent and balanced activities toward both D3 dopamine receptor and fatty acid amide hydrolase (FAAH) enzyme. By concurrently modulating these targets, our compounds hold great potential toward exerting a disease-modifying effect on nicotine addiction and other forms of compulsive behavior.

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