30711-40-1 Usage
Uses
Used in Pharmaceutical Industry:
2-(N-Heptanoyl)thiophene is used as a pharmaceutical compound for its potential therapeutic properties. The heptanoyl group's attachment to the thiophene molecule may enhance its bioactivity, making it a candidate for drug development in treating various diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(N-Heptanoyl)thiophene is utilized as a component in the development of pesticides or other agrochemical products. The modified properties of the thiophene molecule could provide new ways to target pests or improve crop protection.
Used in Materials Science:
2-(N-Heptanoyl)thiophene is employed in materials science for its potential to contribute to the development of new materials with unique properties. The heptanoyl group's influence on the thiophene molecule could lead to advancements in areas such as polymers, sensors, or electronic materials.
Check Digit Verification of cas no
The CAS Registry Mumber 30711-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,1 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30711-40:
(7*3)+(6*0)+(5*7)+(4*1)+(3*1)+(2*4)+(1*0)=71
71 % 10 = 1
So 30711-40-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H16OS/c1-2-3-4-5-7-10(12)11-8-6-9-13-11/h6,8-9H,2-5,7H2,1H3
30711-40-1Relevant articles and documents
1,3-Dithiane polymers for the supported synthesis of ketones
Bertini, Vincenzo,Lucchesini, Francesco,Pocci, Marco,De Munno, Angela
, p. 9263 - 9266 (2007/10/03)
The synthesis of polymeric reagents containing an odorless propane-1,3- dithiol functionality is reported. Their usefulness for the solid phase synthesis of ketones via the umpoled alkylation of 1,3-dithianes is demonstrated.
DIMETHYLALUMINIUM METHANESELENOLATE - A USEFUL REAGENT FOR THE PREPARATION OF SELENOESTERS. A NEW FRIEDEL-CRAFTS ACYLATION PROCEDURE PROMOTED BY Cu(I)
Kozikowski, Alan P.,Ames, Anthony
, p. 4821 - 4834 (2007/10/02)
The preparation of a new aluminium reagent, dimethylaluminium methaneselenolate (Me2AlSeMe) is described.The reactivity of this aluminium reagent toward a variety of organic substrates has been studied.Me2AlSeMe will convert O-alkyl esters to selenoesters in high yield.These selenoesters function as extremely reactive acyl transfer agents and are converted to acids, esters, and amides on reaction with water, alcohols or amines in the presence of a selenophilic metal cation.The selenoesters will, moreover, acylate reactive arenes and heterocyclic compounds when cuprous triflate is employed as the selenophilic metal cation.This latter transformation constitutes a new transition metal promoted variant of the Friedel-Crafts acylation reaction.
