14109-72-9 Usage
Description
1-METHYLTHIO-2-PROPANONE, also known as MTP, is an organic compound that serves as a crucial intermediate in various chemical syntheses. It is characterized by its distinct melon-like odor and is widely recognized for its applications across different industries due to its unique chemical properties.
Uses
Used in Organic Synthesis:
1-METHYLTHIO-2-PROPANONE is used as a key intermediate for the synthesis of various organic compounds. Its unique structure allows for the creation of a broad range of products, making it a valuable asset in the field of organic chemistry.
Used in Pharmaceutical Industry:
1-METHYLTHIO-2-PROPANONE is used as a building block in the development of new pharmaceuticals. Its versatility in chemical reactions enables the production of diverse drug candidates, contributing to the advancement of medical treatments.
Used in Agrochemicals:
1-METHYLTHIO-2-PROPANONE is utilized as a vital component in the formulation of agrochemicals. Its role in creating effective pesticides and other agricultural products helps improve crop protection and yield.
Used in Dyestuff Industry:
1-METHYLTHIO-2-PROPANONE is employed as a raw material in the production of dyes and pigments. Its chemical properties facilitate the creation of a wide array of colorants, catering to the needs of various industries that rely on dyestuffs for coloring textiles, plastics, and other materials.
Check Digit Verification of cas no
The CAS Registry Mumber 14109-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14109-72:
(7*1)+(6*4)+(5*1)+(4*0)+(3*9)+(2*7)+(1*2)=79
79 % 10 = 9
So 14109-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H8OS/c1-4(5)3-6-2/h3H2,1-2H3
14109-72-9Relevant articles and documents
Anomalous Hydrogen-Deuterium Exchange of Cyclic β-Keto Sulfides
Guth, Jacob J.,Gross, Rosalind L.,Carson, Frederick W.
, p. 2666 - 2668 (1982)
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A biocatalytic route to enantioenriched, sulfanyl aldol products
Baker-Glenn,Ancliff,Gouverneur
, p. 7607 - 7619 (2007/10/03)
The aldol products derived from sulfur- or selenium containing acceptors were prepared by kinetic resolution in the presence of antibody 84G3 with enantiomeric excesses ranging from 56 to 70%. Much higher level of enantioselectivity was obtained (enantiomeric excesses all superior to 96%) for sulfanyl aldol products derived from thiomethoxyacetone with three different acceptors.
Substituted indoles as alpha-1 agonists
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, (2008/06/13)
This invention relates to compounds which are alpha-1 receptor agonists, preferably alpha-1A/L receptor agonists, and which are represented by Formula I: wherein X is —S(O)n— or —C(O)—, A is C1-6alkyl, aryl, heteroaryl, hydroxyalkyl,
New hypoxia-selective cytotoxines derived from quinoxaline 1,4-dioxides
Monge,Palop,Gonzalez,Martinez-Crespo,Lopez De Cerain,Sainz,Narro,Barker,Hamilton
, p. 1213 - 1217 (2007/10/02)
A new series of quinoxaline 1,4-dioxides, structurally related to the benzotriazine tirapazamine 1 have been prepared starting from 5,6-dichlorobenzofuroxane 2. The Beirut reaction between 2 and alkyl or aryl thiopropanones afforded the 2-methyl-3-alkyl(a