4083-85-6 Usage
Description
(Ethoxycarbonylmethyl)triphenylphosphonium bromide, with the chemical formula C24H25BrO3P, is a quaternary ammonium compound characterized by its white crystalline solid appearance. It is soluble in polar solvents such as methanol and ethanol, and is renowned for its ability to act as a phase-transfer catalyst in organic synthesis. This unique property allows it to facilitate the transfer of reactants from one phase to another, thereby enhancing the efficiency of certain chemical reactions. Its potential applications in various organic transformations have garnered significant attention within the scientific community.
Uses
Used in Pharmaceutical Synthesis:
(Ethoxycarbonylmethyl)triphenylphosphonium bromide is utilized as a phase-transfer catalyst in the synthesis of pharmaceuticals. Its ability to improve the efficiency of chemical reactions aids in the production of various medicinal compounds.
Used in Agrochemical Synthesis:
In the agrochemical industry, (Ethoxycarbonylmethyl)triphenylphosphonium bromide is employed for a similar purpose, acting as a phase-transfer catalyst to enhance the synthesis of agrochemicals, which includes pesticides and other products used in agriculture.
Used in Fine Chemicals Synthesis:
(ETHOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM BROMIDE is also used in the synthesis of fine chemicals, which are high-purity chemicals used in various applications such as fragrances, dyes, and electronic materials. The phase-transfer catalytic properties of (Ethoxycarbonylmethyl)triphenylphosphonium bromide contribute to the efficiency and effectiveness of these chemical reactions.
Overall, (Ethoxycarbonylmethyl)triphenylphosphonium bromide is a versatile compound with significant applications across different industries, primarily due to its role as a phase-transfer catalyst in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 4083-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4083-85:
(6*4)+(5*0)+(4*8)+(3*3)+(2*8)+(1*5)=86
86 % 10 = 6
So 4083-85-6 is a valid CAS Registry Number.
4083-85-6Relevant articles and documents
Chemo-enzymatic synthesis of specifically stable-isotope labelled L-glutamic acid and 2-oxoglutaric acid
Cappon, J. J.,Baart, J.,Walle, G. A. M. van der,Raap, J.,Lugtenburg, J.
, p. 158 - 166 (2007/10/02)
(3-13C)-(4-13C)-,(5-13C)- and (3,4-13C2)-2-oxoglutaric acid were prepared starting from the simple 13C-enriched compounds: ethyl bromoacetate and paraformaldehyde, via a single reaction scheme on the gram scale in high yield.This reaction scheme allows specific 13C enrichment of every carbon position and any combination of positions. (3-13C)-,(4-13C)-, (5-13C), (3,4-13C2) and (15N)-L-glutamic acid were prepared by converting the corresponding 2-oxoglutaric acids via an enantioselective enzymatic conversion.The labelled L-glutamic acids and 2-oxoglutaric acids were characterized by 1H NMR, 13C NMR and mass spectrometry.
