102438-91-5 Usage
Uses
Used in Pharmaceutical Industry:
(3-Propylpyridin-2-yl)methanol is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into drug molecules, potentially enhancing their therapeutic properties and efficacy.
Used in Agrochemical Industry:
In the agrochemical field, (3-Propylpyridin-2-yl)methanol serves as a vital component in the development of novel pesticides and other crop protection agents. Its chemical properties can be leveraged to create more effective and targeted agrochemicals.
Used in Material Science:
(3-Propylpyridin-2-yl)methanol is utilized in the development of innovative materials, such as polymers and coatings, due to its reactive functional groups and compatibility with various other chemical compounds.
Used in Research and Development:
As a pyridine derivative with a propyl group and hydroxyl group, (3-Propylpyridin-2-yl)methanol is an important compound in academic and industrial research. It is used to explore new chemical reactions, investigate its potential applications, and develop new methodologies for organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 102438-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,3 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102438-91:
(8*1)+(7*0)+(6*2)+(5*4)+(4*3)+(3*8)+(2*9)+(1*1)=95
95 % 10 = 5
So 102438-91-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c1-2-4-8-5-3-6-10-9(8)7-11/h3,5-6,11H,2,4,7H2,1H3
102438-91-5Relevant academic research and scientific papers
Discovery of functionally selective 7,8,9,10-tetrahydro-7,10-ethano-1,2,4- triazolo[3,4-a]phthalazines as GABAA receptor agonists at the α3 subunit
Russell, Michael G. N.,Carling, Robert W.,Atack, John R.,Bromidge, Frances A.,Cook, Susan M.,Hunt, Peter,Isted, Catherine,Lucas, Matt,McKernan, Ruth M.,Mitchinson, Andrew,Moore, Kevin W.,Narquizian, Robert,Macaulay, Alison J.,Thomas, David,Thompson, Sally-Anne,Wafford, Keith A.,Castro, José L.
, p. 1367 - 1383 (2007/10/03)
We have previously identified the 7,8,9,10-tetrahydro-7,10-ethano-1,2,4- triazolo[3,4-a]phthalazine (1) as a potent partial agonist for the 0.3 receptor subtype with 5-fold selectivity in binding affinity over α1. This paper describes a detailed investigation of the substituents on this core structure at both the 3- and 6-positions. Despite evaluating a wide range of groups, the maximum selectivity that could be achieved in terms of affinity for the α3 subtype over the α1 subtype was 12-fold (for 57). Although most analogues showed no selectivity in terms of efficacy, some did show partial agonism at α1 and antagonism at α3 (e.g., 25 and 75). However, two analogues tested (93 and 96), both with triazole substituents in the 6-position, showed significantly higher efficacy for the α3 subtype over the α1 subtype. This was the first indication that selectivity in efficacy in the required direction could be achieved in this series.
