35835-94-0 Usage
Description
Ethyltriphenylphosphonium acetate is a versatile chemical compound composed of a triphenylphosphonium cation and an acetate anion. It is recognized for its strong basic and nucleophilic properties, which facilitate the formation of carbon-carbon and carbon-heteroatom bonds. Ethyltriphenylphosphonium acetate plays a significant role in organic synthesis and pharmaceutical research, particularly in the synthesis of biologically active compounds and as a reagent in various organic reactions, highlighting its importance in the field of organic chemistry.
Uses
Used in Organic Synthesis:
Ethyltriphenylphosphonium acetate is used as a precursor in organic synthesis for its ability to form carbon-carbon and carbon-heteroatom bonds, which is crucial in creating complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, Ethyltriphenylphosphonium acetate is utilized as a reagent in the synthesis of biologically active compounds, contributing to the development of new drugs and therapeutic agents.
Used in the Synthesis of Organic Compounds:
Ethyltriphenylphosphonium acetate is employed as a reagent in the synthesis of a wide range of organic compounds due to its structure and reactivity, making it an indispensable tool in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 35835-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,3 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35835-94:
(7*3)+(6*5)+(5*8)+(4*3)+(3*5)+(2*9)+(1*4)=140
140 % 10 = 0
So 35835-94-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H20P.C2H4O2/c1-2-21(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20;1-2(3)4/h3-17H,2H2,1H3;1H3,(H,3,4)/q+1;/p-1
35835-94-0Relevant articles and documents
Wittig Olefination Using Phosphonium Ion-Pair Reagents Incorporating an Endogenous Base
Vetter, Anna C.,Gilheany, Declan G.,Nikitin, Kirill
supporting information, p. 1457 - 1462 (2021/03/08)
Despite common perception, the use of strong bases in Wittig chemistry is utterly unnecessary: we report a series of novel ion-pair phosphonium carboxylate reagents which are essentially "storable ylides". These reagents are straightforwardly prepared in excellent yields, and their fluxional nature permits clean olefination of a broad range of aldehydes and even hemiacetals.