4083-85-6 Usage
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 academic research and scientific papers
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.
