54882-04-1 Usage
Description
Phenylsulfinylacetic acid ethyl ester, with the molecular formula C10H12O3S, is a colorless, aromatic liquid that is soluble in organic solvents. It is an ethyl ester of phenylsulfinylacetic acid and is widely recognized for its versatility in organic synthesis, particularly in the synthesis of pharmaceuticals and other organic compounds. Its ability to participate in a range of chemical reactions and serve as a building block in the creation of complex molecules underscores its significance in the realm of organic chemistry.
Uses
Used in Organic Synthesis:
Phenylsulfinylacetic acid ethyl ester is used as a reagent in organic synthesis for its capacity to undergo various chemical reactions, contributing to the formation of a wide array of organic compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, phenylsulfinylacetic acid ethyl ester is utilized as a key intermediate in the synthesis of various drugs, highlighting its importance in medicinal chemistry.
Used in Building Complex Molecules:
Phenylsulfinylacetic acid ethyl ester is employed as a building block in the assembly of complex molecules, which is crucial for the advancement of novel chemical entities and materials in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 54882-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,8 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54882-04:
(7*5)+(6*4)+(5*8)+(4*8)+(3*2)+(2*0)+(1*4)=141
141 % 10 = 1
So 54882-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3S/c1-2-13-10(11)8-14(12)9-6-4-3-5-7-9/h3-7H,2,8H2,1H3
54882-04-1Relevant articles and documents
Byproduct formation during the biosynthesis of spinosyn A and evidence for an enzymatic interplay to prevent its formation
Choi, Sei-hyun,Franklin, Joseph Livy,Huang, Teng-Yi,Hung, Shang-Cheng,Jeon, Byung-sun,Kim, Namho,Liu, Hung-wen,Ruszczycky, Mark W.
supporting information, (2021/11/30)
Biosynthesis of spinosyn A in Saccharopolyspora spinosa involves a 1,4-dehydration followed by an intramolecular [4 + 2]-cycloaddition catalyzed by SpnM and SpnF, respectively. The cycloaddition also takes place in the absence of SpnF leading to questions
Synthesis of: N -alkylated 2-pyridones through Pummerer type reactions of activated sulfoxides and 2-fluoropyridine derivatives
Hu, Gang,Xu, Jiaxi,Li, Pingfan
, p. 4151 - 4158 (2018/06/12)
N-Alkylated 2-pyridone products were obtained in good to excellent yields through a one-pot procedure involving either normal or interrupted Pummerer reactions between triflic anhydride activated sulfoxides and 2-fluoropyridine derivatives, followed by hydrolysis. This is a rare case that uses 2-fluoropyridine as a nucleophile in Pummerer type reactions.
Ammonium salt catalyzed oxidation of organosulfides to organosulfoxydes
Secci, Francesco,Frongia, Angelo,Piras, Pier Paolo
, p. 603 - 605 (2014/01/23)
The selective oxidation of aromatic and aliphatic organosulfides with H2O2/H2O catalyzed by metal free ammonium salts has been explored. Reactions were performed using 2.5-5 mol % of catalyst loadings, isolating the corres
