31704-82-2 Usage
Description
4-methyl-4-(5-methyl-2-furyl)pentan-2-one is an organic compound that features a pentan-2-one backbone with methyl and furyl substituents. It is characterized by its unique structure and properties, making it a versatile intermediate in organic synthesis.
Uses
Used in Chemical Synthesis:
4-methyl-4-(5-methyl-2-furyl)pentan-2-one is used as a key intermediate in the synthesis of trifluoromethyl derivatives of furan and other related derivatives. Its unique structure allows for the introduction of trifluoromethyl groups, which are important in various applications due to their unique reactivity and properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-methyl-4-(5-methyl-2-furyl)pentan-2-one is used as a building block for the development of novel drug candidates. Its ability to form trifluoromethyl derivatives makes it a valuable component in the design of new molecules with potential therapeutic applications.
Used in Agrochemical Industry:
4-methyl-4-(5-methyl-2-furyl)pentan-2-one is also utilized in the agrochemical industry for the synthesis of new pesticides and agrochemicals. The trifluoromethyl derivatives of furan that can be prepared using this compound may exhibit enhanced biological activity and selectivity, making them valuable in crop protection and pest control.
Overall, 4-methyl-4-(5-methyl-2-furyl)pentan-2-one is a versatile and valuable compound in various industries, particularly in chemical synthesis, pharmaceuticals, and agrochemicals, due to its potential in the preparation of trifluoromethyl derivatives and other related compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 31704-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,0 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31704-82:
(7*3)+(6*1)+(5*7)+(4*0)+(3*4)+(2*8)+(1*2)=92
92 % 10 = 2
So 31704-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O2/c1-8(12)7-11(3,4)10-6-5-9(2)13-10/h5-6H,7H2,1-4H3
31704-82-2Relevant articles and documents
A diesel oil or aviation kerosene cyclanes for process for the preparation of (by machine translation)
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Paragraph 0049; 0050; 0051; 0052; 0053; 0054, (2017/07/22)
The invention is in the field of organic synthesis, relates to a diesel oil or aviation kerosene cyclanes for the preparation method. Method is as follows: 1) lignocellulolytic yl furan compound and carbonyl compound is subjected to acid or alkali catalys
Gold(III) Chloride-Catalyzed Addition Reactions of Electron-Rich Arenes to Methyl Vinyl Ketone
Dyker, Gerald,Muth, Enrico,Hashmi, A. Stephen K.,Ding, Li
, p. 1247 - 1252 (2007/10/03)
For the reaction of α,β-unsaturated ketones with electron-rich arenes catalyzed by gold(III) chloride both, a Friedel-Crafts-type mechanism and an initial metallation, are evaluated. Gold(III) chloride has proven to be an efficient catalyst under very mod
THE BF3-CATALYSED REACTION BETWEEN 2-METHYLFURAN AND SOME α,β-UNSATURATED CARBONYL COMPOUNDS.
ApSimon, J.,Srinivasan, V. Seenu,L'Abbe, M. R.,Seguin, R.
, p. 1079 - 1081 (2007/10/02)
The reaction of 2-methylfuran with some αβ unsaturated compounds in the presence of BF3-etherate is described as well as studies of the cleavage of the furan ring of the products.Only 1,4-addition to the conjugated carbonyl system is observed even in the
