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[3-[[(PYRIDIN-4-YL)THIO]METHYL]PHENYL]METHANOL is a chemical compound characterized by its molecular formula C16H15NOS. It is a thioether that features a pyridine ring, a phenyl group, and a methanol moiety. [3-[[(PYRIDIN-4-YL)THIO]METHYL]PHENYL]METHANOL's structural diversity and functional groups make it a promising candidate for various applications in pharmaceuticals, agrochemicals, and materials science. The pyridine ring may contribute to its biological activity, while the thioether and phenyl groups serve as valuable building blocks for organic synthesis. Additionally, the methanol group may offer solubility and reactivity benefits in specific chemical reactions. The unique combination of features in [3-[[(PYRIDIN-4-YL)THIO]METHYL]PHENYL]METHANOL makes it an intriguing compound for further research and potential use across different industrial and scientific fields.

811801-40-8

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811801-40-8 Usage

Uses

Used in Pharmaceutical Industry:
[3-[[(PYRIDIN-4-YL)THIO]METHYL]PHENYL]METHANOL is used as a potential pharmaceutical compound for its possible biological activity. The presence of the pyridine ring may allow it to interact with various biological targets, making it a candidate for drug development.
Used in Agrochemical Industry:
In the agrochemical industry, [3-[[(PYRIDIN-4-YL)THIO]METHYL]PHENYL]METHANOL may be utilized as a building block for the synthesis of new agrochemicals, potentially offering novel modes of action or improved properties compared to existing products.
Used in Materials Science:
[3-[[(PYRIDIN-4-YL)THIO]METHYL]PHENYL]METHANOL's structural features and functional groups can be exploited in materials science to develop new materials with specific properties. [3-[[(PYRIDIN-4-YL)THIO]METHYL]PHENYL]METHANOL's thioether and phenyl groups, along with its methanol moiety, may contribute to the creation of materials with unique characteristics for various applications.
Overall, [3-[[(PYRIDIN-4-YL)THIO]METHYL]PHENYL]METHANOL's diverse structural elements and potential applications across different industries highlight its importance as a compound of interest for further investigation and development.

Check Digit Verification of cas no

The CAS Registry Mumber 811801-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,1,8,0 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 811801-40:
(8*8)+(7*1)+(6*1)+(5*8)+(4*0)+(3*1)+(2*4)+(1*0)=128
128 % 10 = 8
So 811801-40-8 is a valid CAS Registry Number.

811801-40-8SDS

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 [3-(pyridin-4-ylsulfanylmethyl)phenyl]methanol

1.2 Other means of identification

Product number -
Other names -

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:811801-40-8 SDS

811801-40-8Downstream Products

811801-40-8Relevant academic research and scientific papers

Allosteric potentiators of the metabotropic glutamate receptor 2 (mGlu2). Part 2: 4-Thiopyridyl acetophenones as non-tetrazole containing mGlu2 receptor potentiators

Pinkerton, Anthony B.,Cube, Rowena V.,Hutchinson, John H.,James, Joyce K.,Gardner, Michael F.,Schaffhauser, Hervé,Rowe, Blake A.,Daggett, Lorrie P.,Vernier, Jean-Michel

, p. 5867 - 5872 (2007/10/03)

We have identified and synthesized a series of 4-thiopyridyl acetophenones as positive allosteric potentiators of the metabotropic glutamate receptor 2. Structure-activity relationship studies directed toward replacement of the tetrazole in the initial lead led to the discovery of 16 (EC50 = 340 nM), which showed improved brain penetration over the initial lead. We have identified and synthesized a series of 4-thiopyridyl acetophenones as positive allosteric potentiators of the metabotropic glutamate receptor 2. Structure-activity relationship studies directed toward replacement of the tetrazole in the initial lead led to the discovery of 16 (EC50 = 340 nM), which showed improved brain penetration over the initial lead.

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