17027-69-9 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-BIPHENYL)ETHYLAMINE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-BIPHENYL)ETHYLAMINE is utilized as a precursor in the production of agrochemicals, aiding in the creation of compounds that can protect crops and enhance agricultural productivity.
Used in Dye Production:
2-(4-BIPHENYL)ETHYLAMINE is used as a precursor in the production of dyes, where its aromatic structure contributes to the color and stability of the dyes in various applications.
Used in Polymer Synthesis:
2-(4-BIPHENYL)ETHYLAMINE is also used as a monomer or a building block in the synthesis of polymers, where its chemical structure can influence the polymer's properties, such as strength, flexibility, and durability.
Used as a Reagent in Organic Chemistry:
2-(4-BIPHENYL)ETHYLAMINE serves as a reagent in various organic chemistry reactions, facilitating the formation of desired products through its reactive amine group.
Check Digit Verification of cas no
The CAS Registry Mumber 17027-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,2 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17027-69:
(7*1)+(6*7)+(5*0)+(4*2)+(3*7)+(2*6)+(1*9)=99
99 % 10 = 9
So 17027-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N/c1-8-3-4-10(5-6-11)9(2)7-8/h3-4,7H,5-6,11H2,1-2H3
17027-69-9Relevant academic research and scientific papers
New N-arachidonoylserotonin analogues with potential "dual" mechanism of action against pain
Ortar, Giorgio,Cascio, Maria Grazia,De Petrocellis, Luciano,Morera, Enrico,Rossi, Francesca,Schiano-Moriello, Aniello,Nalli, Marianna,De Novellis, Vito,Woodward, David F.,Maione, Sabatino,Di Marzo, Vincenzo
, p. 6554 - 6569 (2008/09/17)
N-Arachidonoylserotonin (AA-5-HT, 1a) is an inhibitor of fatty acid amide hydrolase (FAAH) that acts also as an antagonist of transient receptor potential vanilloid-type 1 (TRPV1) channels and is analgesic in rodents. We modified the chemical structure of 1a with the aim of developing "hybrid" FAAH/TRPV1 blockers more potent than the parent compound or obtaining analogues with single activity at either of the two targets to study the mechanism of the analgesic action of 1a. Thirty-eight AA-5-HT analogues, containing a serotonin "head" bound to a variety of lipophilic moieties via amide, urea, or carbamate functionalities, were synthesized. Unlike 1a, most of the new compounds possessed activity at only one of the two considered targets. The amides 1b and 1c of α- and γ-linolenic acid, however, showed "hybrid" activity similar to 1a. The carbamate 3f (OMDM106), although unable to antagonize TRPV1 receptors, was the most potent FAAH inhibitor in this study (IC50 = 0.5 μM). Compounds 3f and 1m (OMDM129), which exhibited activity at only FAAH or TRPV1, respectively, were 10-fold less potent than 1a at preventing formalin-induced hyperalgesia in mice.
