201008-67-5 Usage
Uses
Used in Organic Synthesis:
3,5-DIMETHYL-4-(1,3-DITHIAN-YL)-1-PHENYLPYRAZOLE is used as a synthetic building block for the development of new organic compounds. Its application in this field is due to its versatile chemical properties, which allow for the creation of a wide range of molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,5-DIMETHYL-4-(1,3-DITHIAN-YL)-1-PHENYLPYRAZOLE is used as a key intermediate in the synthesis of various drugs. Its unique structure and reactivity make it a valuable component in the development of new medications with improved efficacy and reduced side effects.
Used in Chemical Research:
3,5-DIMETHYL-4-(1,3-DITHIAN-YL)-1-PHENYLPYRAZOLE is also used as a research tool in the field of chemistry. Its distinctive properties make it an interesting subject for studying various chemical reactions and mechanisms, contributing to the advancement of knowledge in the field.
Used in Material Science:
In the field of material science, 3,5-DIMETHYL-4-(1,3-DITHIAN-YL)-1-PHENYLPYRAZOLE is used as a component in the development of novel materials with specific properties. Its unique chemical structure allows for the creation of materials with potential applications in various industries, such as electronics, energy, and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 201008-67-5 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 201008-67:
(8*2)+(7*0)+(6*1)+(5*0)+(4*0)+(3*8)+(2*6)+(1*7)=65
65 % 10 = 5
So 201008-67-5 is a valid CAS Registry Number.
201008-67-5Relevant 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.
