22002-73-9 Usage
Uses
Used in Organic Synthesis:
3-(n-Butylsulphanyl)propionic acid serves as a valuable building block in organic synthesis, contributing to the creation of a wide range of chemical compounds. Its structural features facilitate the formation of carbon-carbon and carbon-sulfur bonds, which are crucial in the development of new molecules with specific functionalities.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 3-(n-Butylsulphanyl)propionic acid is utilized as a key intermediate in the synthesis of various drugs. Its unique chemical properties allow for the development of therapeutic agents with novel mechanisms of action, potentially leading to the discovery of new treatments for a variety of diseases.
Used in Agrochemical Industry:
3-(n-Butylsulphanyl)propionic acid also finds application in the agrochemical industry, where it is employed in the synthesis of pesticides and other crop protection agents. Its reactivity and structural attributes enable the creation of compounds with enhanced efficacy and selectivity, contributing to more effective and environmentally friendly agricultural practices.
Used as a Reagent in Chemical Reactions:
3-(n-Butylsulphanyl)propionic acid functions as a reagent in various chemical reactions, particularly those involving the formation of carbon-carbon and carbon-sulfur bonds. Its presence in these reactions can improve the yield and selectivity of the desired products, making it an indispensable tool in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 22002-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,0 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22002-73:
(7*2)+(6*2)+(5*0)+(4*0)+(3*2)+(2*7)+(1*3)=49
49 % 10 = 9
So 22002-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2S/c1-2-3-5-10-6-4-7(8)9/h2-6H2,1H3,(H,8,9)
22002-73-9Relevant academic research and scientific papers
An improved and green preparation of 3-(alkylthio)propionic acids
Vaismaa, Matti J. P.,Yliniemel?, Sanna M.,Lajunen, Marja K.
, p. 1317 - 1323 (2008/10/09)
An efficient, facile microwave-assisted synthesis has been developed for the preparation of unsymmetrical sulfide derivatives from 3-mercaptopropionic acid and a wide variety of alkyl, allyl or aryl chlorides or bromides. The synthesis performed in ethanol at 80 or 120 °C using sodium hydroxide as a base, selectively without an offensive smell, generates 3-(alkylthio)propionic acids in good yields. Effects of reaction components, temperature, and the heating technique on the formation of the product and side-products were studied.
S,S-Dialkyl Dithiocarbonates as a Convenient Source of Alkanethiols: an Improved Synthesis of Alkylthiocarboxylic Acids
Cadamuro, Silvano,Degani, Iacopo,Fochi, Rita,Regondi, Valeria
, p. 1070 - 1074 (2007/10/02)
A wide variety of β-alkylthiocarboxylic acids are obtained by addition of alkanethiols - generated in situ from S,S-dialkyl dithiocarbonates - to appropriate α,β-unsaturated carboxylic acids in good to excellent yields.
