18325-74-1 Usage
Description
ETHYL-2-(3-ALLYL)-4-PENTENOATE, also known as Diallylacetic Acid Ethyl Ester, is an organic compound with a molecular structure that features an ester functional group. It is characterized by its reactivity and ability to participate in various chemical reactions, making it a versatile compound in the field of organic chemistry.
Uses
Used in Chemical Synthesis:
ETHYL-2-(3-ALLYL)-4-PENTENOATE is used as a reactant for the synthesis of isopentenyl-N-methylquinolinedione. This application takes advantage of its reactivity and ability to form new chemical bonds, contributing to the creation of complex organic molecules with potential applications in various industries.
If there are additional applications in different industries, they can be listed as follows:
Used in Pharmaceutical Industry:
ETHYL-2-(3-ALLYL)-4-PENTENOATE could potentially be used as an intermediate in the synthesis of pharmaceutical compounds, given its reactivity and ability to form new chemical bonds. This application would leverage its chemical properties to develop new drugs with specific therapeutic effects.
Used in Flavor and Fragrance Industry:
Due to its unique chemical structure, ETHYL-2-(3-ALLYL)-4-PENTENOATE may also find use in the flavor and fragrance industry as a component in the creation of various scents and flavors. Its ability to participate in chemical reactions could be harnessed to produce novel and distinct sensory experiences.
Check Digit Verification of cas no
The CAS Registry Mumber 18325-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,2 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18325-74:
(7*1)+(6*8)+(5*3)+(4*2)+(3*5)+(2*7)+(1*4)=111
111 % 10 = 1
So 18325-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2/c1-4-7-9(8-5-2)10(11)12-6-3/h4-5,9H,1-2,6-8H2,3H3
18325-74-1Relevant articles and documents
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McElvain,Kundiger
, p. 254,259 (1942)
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Combined dealkoxycarbonylation and lactonisation of unsaturated malonates in ionic liquids
Oswald, Magalie F.,Parsons, Andrew F.,Yang, Wei,Bowden, Martin
, p. 8087 - 8089 (2007/10/03)
Heating unsaturated malonates with LiCl and water in [bmim][Br] or [bmim][BF4]/[bmim][Br] produces unsaturated esters or lactones, respectively.
Synthesis and Supramolecular Properties of Conformationally Restricted and Flexible Phospholipids
Vares, Lauri,Koulov, Atanas V.,Smith, Bradley D.
, p. 10073 - 10078 (2007/10/03)
Short synthetic routes are described to produce structurally related phospholipids that are either conformationally restricted or flexible. The conformationally restricted structures have a cyclopropyl ring in the interfacial region of the phospholipid. T
