50690-55-6 Usage
Uses
Used in Pharmaceutical Industry:
[p-(Pentyloxy)phenyl]acetonitrile is used as a pharmaceutical intermediate for the synthesis of various drugs and active pharmaceutical ingredients. Its unique chemical structure allows it to be a versatile building block in the development of new medications.
Used in Research and Development:
PPAP is used as a research compound in the field of psychopharmacology. It is utilized to study the effects of novel psychoactive substances on the central nervous system and to understand their potential therapeutic applications in mental health disorders.
Used in Chemical Synthesis:
[p-(Pentyloxy)phenyl]acetonitrile is used as a chemical intermediate in the synthesis of various organic compounds. Its reactivity and functional groups make it a valuable component in the production of specialty chemicals, agrochemicals, and other industrial products.
Used in Drug Discovery:
PPAP is used as a lead compound in drug discovery programs. Its unique pharmacological profile and potential therapeutic effects make it a promising candidate for the development of new drugs targeting mental health disorders and other conditions.
Used in Toxicological Studies:
[p-(Pentyloxy)phenyl]acetonitrile is used in toxicological studies to evaluate the safety and potential side effects of novel psychoactive substances. Understanding its toxicological profile is crucial for assessing its suitability as a therapeutic agent and for ensuring the safety of its use in humans.
Check Digit Verification of cas no
The CAS Registry Mumber 50690-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,9 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50690-55:
(7*5)+(6*0)+(5*6)+(4*9)+(3*0)+(2*5)+(1*5)=116
116 % 10 = 6
So 50690-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO/c1-2-3-4-11-15-13-7-5-12(6-8-13)9-10-14/h5-8H,2-4,9,11H2,1H3
50690-55-6Relevant academic research and scientific papers
Synthesis and thermal properties of twin dimers containing cyanostilbene derivatives as a mesogenic group
Mihara,Ito,Koide
, p. 69 - 85 (2007/10/03)
We synthesized twin dimers (TDs) with different linking groups between a mesogenic group and a flexible spacer, different spacer length, and different terminal alkyl chain length to clarify the effect of these groups on the mesomorphic properties of the T
Design of Inhibitors from the Three-Dimensional Structure of Alcohol Dehydrogenase. Chemical Synthesis and Enzymatic Properties
Freudenreich, Charles,Samama, Jean-Pierre,Biellmann, Jean-Francois
, p. 3344 - 3353 (2007/10/02)
Inhibitors of liver alcohol dehydrogenase were designed from the three-dimensional structure of the enzyme.The ligand to the catalytic zinc ion is an amide group or, better, a formamide group.With the latter function, a hydrogen bond between the NH group and the hydroxyl group of Ser-48 may be formed.The hydrophobic substrate binding site brings structural restraints. α-ω bifunctional molecules show good inhibitory properties possibly due to the interactions with polar residues at the entrance of the substrate binding site.
