30698-17-0 Usage
Description
[3-(acetyloxy)propyl](triphenyl)phosphonium, with the chemical formula C25H25O2P, is a phosphonium salt that serves as a reactant in organic synthesis. [3-(acetyloxy)propyl](triphenyl)phosphonium features a phosphonium group, a propyl group with an acetyloxy substituent, and three phenyl groups. The acetyloxy group is a functional group capable of engaging in various chemical reactions, while the phosphonium group, being positively charged, can function as an electrophile in reactions.
Uses
Used in Organic Synthesis:
[3-(acetyloxy)propyl](triphenyl)phosphonium is used as a reactant for the development of new synthetic methodologies in the field of organic chemistry. Its unique structure allows for a wide range of applications in creating diverse organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [3-(acetyloxy)propyl](triphenyl)phosphonium is used as a reagent for the preparation of various organic compounds. Its ability to act as an electrophile and participate in different chemical reactions makes it a valuable tool in the synthesis of pharmaceutically relevant molecules.
Used in Chemical Research:
[3-(acetyloxy)propyl](triphenyl)phosphonium is also utilized in chemical research as a compound that can help scientists understand and develop new reaction mechanisms and pathways. Its versatile nature allows for exploration in various areas of chemistry, potentially leading to new discoveries and advancements.
Check Digit Verification of cas no
The CAS Registry Mumber 30698-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,9 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30698-17:
(7*3)+(6*0)+(5*6)+(4*9)+(3*8)+(2*1)+(1*7)=120
120 % 10 = 0
So 30698-17-0 is a valid CAS Registry Number.
30698-17-0Relevant articles and documents
Pheromones, 57.- Synthesis of Lepidoptera Polyene Pheromones and of Structural Analogs.- Acetylenic Synthesis, Wittig Olefination, and Kolbe Electrolysis
Bestmann, Hans Juergen,Roth, Kurt,Michaelis, Karl,Vostrowsky, Otto,Schaefer, Hans J.,Michaelis, Ralf
, p. 417 - 422 (2007/10/02)
By a combination of acetylenic syntheses with Wittig olefination as well as by mixed Kolbe electrolysis alkadienes, alkatrienes, and alkatetraenes (sex attractants of Lepidoptera and structural analogs)were synthesized.
