63547-23-9 Usage
Description
ACETIC ACID, [(DIPHENYLMETHYL)THIO]-, ETHYL ESTER, also known as [(Diphenylmethyl)thio]acetic Acid Ethyl Ester (CAS# 63547-23-9), is a chemical compound that plays a significant role in organic synthesis. It is characterized by its unique structure, which includes a diphenylmethyl group connected to a thioether linkage and an ester functional group derived from acetic acid and ethanol. This versatile compound is known for its potential applications in various industries, making it a valuable component in the field of organic chemistry.
Uses
Used in Organic Synthesis:
ACETIC ACID, [(DIPHENYLMETHYL)THIO]-, ETHYL ESTER is used as a key intermediate in organic synthesis for the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows it to participate in a wide range of chemical reactions, making it a valuable building block for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ACETIC ACID, [(DIPHENYLMETHYL)THIO]-, ETHYL ESTER is used as a starting material for the synthesis of various drug candidates. Its ability to form stable intermediates and participate in a variety of chemical reactions makes it an essential component in the development of new medications with potential therapeutic benefits.
Used in Agrochemical Industry:
ACETIC ACID, [(DIPHENYLMETHYL)THIO]-, ETHYL ESTER is also utilized in the agrochemical industry for the synthesis of pesticides, herbicides, and other crop protection agents. Its unique properties enable it to be incorporated into the molecular structures of these chemicals, potentially enhancing their effectiveness and selectivity in controlling pests and weeds.
Used in Specialty Chemicals Industry:
In the specialty chemicals industry, ACETIC ACID, [(DIPHENYLMETHYL)THIO]-, ETHYL ESTER is employed as a versatile building block for the synthesis of various specialty chemicals, such as dyes, fragrances, and other functional materials. Its ability to form stable intermediates and participate in a wide range of chemical reactions makes it a valuable component in the development of innovative products with unique properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 63547-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63547-23:
(7*6)+(6*3)+(5*5)+(4*4)+(3*7)+(2*2)+(1*3)=129
129 % 10 = 9
So 63547-23-9 is a valid CAS Registry Number.
InChI:InChI=1/C17H18O2S/c1-2-19-16(18)13-20-17(14-9-5-3-6-10-14)15-11-7-4-8-12-15/h3-12,17H,2,13H2,1H3
63547-23-9Relevant articles and documents
Preparation method of alkyl sulfide
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Paragraph 0068, (2019/12/02)
The invention relates to a preparation method of alkyl sulfide. The method comprises the following steps: under the protection of nitrogen, sequentially adding transition metal, a nitrogen ligand, a cocatalyst, an oxidant, a solvent, alkane and thiophenol or mercaptan into a reaction tube, carrying out oxidative dehydrogenation coupling reaction at 80-150 DEG C, ending the reaction after 6-48 hours, evaporating the solvent to dryness, and carrying out column chromatography separation to obtain the alkyl sulfide compound. The method is simple in synthesis process, mild in reaction condition, high in yield and easy to industrialize.
Synthesis and determination of the absolute configuration of the enantiomers of modafinil
Prisinzano, Thomas,Podobinski, John,Tidgewell, Kevin,Luo, Min,Swenson, Dale
, p. 1053 - 1058 (2007/10/03)
The asymmetric synthesis of both enantiomers of modafinil, a unique CNS stimulant with a reduced abuse liability, is described. This approach effectively prepares modafinil on a multigram scale in several steps from benzhydrol. The described synthetic route has also been used to produce the more water soluble analogue, adrafinil. X-ray crystallographic analysis on (-)-(diphenylmethanesulfinyl)acetic acid has determined the absolute configuration to be R.
Intramolecular rhodium carbenoid insertions into aromatic C-H bonds. Preparation of 1,3-dihydrothiophene 2,2-dioxides fused onto aromatic rings
Babu, Suresh D.,Hrytsak, Michael D.,Durst, Tony
, p. 1071 - 1076 (2007/10/02)
The preparation of 1-carboalkoxy-1,3-dihydrobenzenothiophene 2,2-dioxides via rhodium acetate or rhodium trifluoro-acetate catalyzed decomposition of α-diazo-β-arylmethanesulfonyl esters is described.The reaction has been extended to yield 1,3-dihydrothiophene 2,2-dioxides fused to the 2,3 position of thiophene and indole, but not of furans.In the latter case products derived from the opening of the furan ring were obtained.Key words: synthesis, 1-carboalkoxy-1,3-dihydrobenzothiophene 2,2-dioxides, intramolecular carbenoid insertions, rhodium acetate catalysis.
