201008-65-3 Usage
Uses
Used in Organic Synthesis:
3,5-DIMETHYL-4-(1,3-DITHIAN-YL)-1H-PYRAZOLE is used as a synthetic intermediate for the production of various organic compounds. Its presence in reactions can facilitate the formation of desired products, making it an essential component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,5-DIMETHYL-4-(1,3-DITHIAN-YL)-1H-PYRAZOLE is used as a key building block for the development of new drugs. Its unique chemical properties allow it to be incorporated into the molecular structures of potential therapeutic agents, contributing to the discovery of novel medications with improved efficacy and safety profiles.
Used in Agrochemical Industry:
3,5-DIMETHYL-4-(1,3-DITHIAN-YL)-1H-PYRAZOLE also finds application in the agrochemical industry, where it serves as a precursor for the synthesis of new pesticides and herbicides. Its ability to be modified and incorporated into various chemical structures makes it a valuable asset in the development of innovative and effective crop protection products.
Used in Specialty Chemicals:
In the specialty chemicals sector, 3,5-DIMETHYL-4-(1,3-DITHIAN-YL)-1H-PYRAZOLE is utilized as a versatile intermediate for the synthesis of a wide range of products, including dyes, fragrances, and other high-value chemicals. Its adaptability in various chemical reactions makes it an indispensable component in the creation of unique and specialized compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 201008-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,0,0 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 201008-65:
(8*2)+(7*0)+(6*1)+(5*0)+(4*0)+(3*8)+(2*6)+(1*5)=63
63 % 10 = 3
So 201008-65-3 is a valid CAS Registry Number.
201008-65-3Relevant academic research and scientific papers
Routes to building blocks for heterocyclic synthesis by reduction of ketene dithioacetals
Mellor, John M.,Schofield, Stephen R.,Korn, Stewart R.
, p. 17151 - 17162 (2007/10/03)
Two general methods have been developed permitting the effective reduction of ketene dithioacetals to give substituted dithianes. Reduction with magnesium in methanol is less reliable than reduction with zinc in acetic acid. The greater inconsistency of magnesium in methanol has been investigated by a cyclic voltammetric study of the substrates. The utility of the dithianes has been successfully illustrated by cyclisations to afford, after deprotection, a variety of heterocyclic aldehydes.
