106366-23-8 Usage
Description
2-(2-Phenethyl)-1-pyrroline, with the CAS number 106366-23-8, is an organic compound that is characterized by its brown oil appearance. It is primarily recognized for its utility in the field of organic synthesis, where it serves as a valuable building block for the creation of more complex molecules and compounds.
Uses
Used in Organic Synthesis:
2-(2-Phenethyl)-1-pyrroline is used as a synthetic building block for the development of various organic compounds. Its unique structure and chemical properties make it a versatile component in the synthesis of a wide range of molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(2-Phenethyl)-1-pyrroline is utilized as a key intermediate in the synthesis of novel drug candidates. Its incorporation into drug molecules can potentially enhance their therapeutic properties, such as improving potency, selectivity, and pharmacokinetic profiles.
Used in Agrochemical Industry:
2-(2-Phenethyl)-1-pyrroline also finds application in the agrochemical industry, where it is employed in the synthesis of new pesticides, herbicides, and other crop protection agents. Its use in this industry can contribute to the development of more effective and environmentally friendly products.
Used in Specialty Chemicals:
In the specialty chemicals sector, 2-(2-Phenethyl)-1-pyrroline is used as a starting material for the production of various high-value chemicals. These can include fragrances, dyes, and other additives that are used across different industries, such as cosmetics, textiles, and plastics.
Check Digit Verification of cas no
The CAS Registry Mumber 106366-23-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,6 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 106366-23:
(8*1)+(7*0)+(6*6)+(5*3)+(4*6)+(3*6)+(2*2)+(1*3)=108
108 % 10 = 8
So 106366-23-8 is a valid CAS Registry Number.
106366-23-8Relevant articles and documents
Ag(I)-Catalyzed Synthesis of Azabicyclic Alkaloid Frameworks from Ketimine-Tethered Ynones: Total Synthesis of Indolizidine 209D
Ho, Hon Eong,James, Michael J.,O'Brien, Peter,Taylor, Richard J. K.,Unsworth, William P.
supporting information, p. 1439 - 1443 (2018/03/09)
An efficient Ag(I)-catalyzed π-acid activation method for the cyclization of cyclic ketimine-tethered ynones is reported. Various nitrogen-containing scaffolds commonly found in bioactive alkaloids can be prepared in high yields, and the utility of the method is demonstrated by a formal synthesis of (±)-lasubine II and in a short total synthesis of (±)-indolizidine 209D.
Boric acid: a new regiospecific decarboxylating agent. Syntheses of cyclic imines, β-enaminones, and β-enaminodiketones from β-enaminoesters
Delbecq, Philippe,Bacos, Daniel,Celerier, Jean Pierre,Lhommet, Gerard
, p. 1201 - 1206 (2007/10/02)
The synthesis of cyclic imines 2, β-enaminones 6, and β-enaminodiketones 7 is described.Regio- and stereospecific thermolysis of β-enaminoesters 4 with boric acid permit these preparations in generally good yields. Key words: boric acid, cyclic β-enaminoesters, decarboxylation, cyclic imines, cyclic β-enaminones.
THE PREPARATION OF "ELONGATED" NICOTINE ANALOGUES
Secor, Henry V.,Seeman, Jeffrey I.
, p. 1687 - 1698 (2007/10/02)
The preparation of four nicotine analogues having one or two additional methylene units between the N-methylpyrrolidinyl moiety and the aromatic ring are reported.Also prepared are the corresponding nornicotine and myosmine analogues.The course of the Spa
