53608-93-8 Usage
Description
Diethyl 2-cyclopenten-1-ylmalonate is an organic compound with the molecular formula C14H20O4. It is a diester derived from malonic acid and features a cyclopentene ring as one of its functional groups. This chemical is widely recognized for its reactivity and its use as a building block in creating more complex molecules, which makes it a valuable intermediate in organic synthesis.
Uses
Used in Pharmaceutical Industry:
Diethyl 2-cyclopenten-1-ylmalonate serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, diethyl 2-cyclopenten-1-ylmalonate is utilized as an intermediate for the production of pesticides and other agrochemicals. Its role in this industry is vital for the creation of effective and targeted solutions for agricultural applications.
Used in Organic Synthesis:
Diethyl 2-cyclopenten-1-ylmalonate is employed as a versatile building block in organic synthesis. Its ability to participate in a range of chemical reactions makes it instrumental in the construction of complex organic molecules for various applications.
Used in Heterocyclic Compound Preparation:
diethyl 2-cyclopenten-1-ylmalonate is also known for its role in the preparation of heterocyclic compounds, which are an integral part of many biologically active molecules and have wide-ranging applications in material science and medicinal chemistry.
Used in Natural Product Synthesis:
Diethyl 2-cyclopenten-1-ylmalonate is utilized in the synthesis of natural products, which often have potent biological activities and are the basis for many drugs and therapeutic agents. Its presence in this field highlights its importance in the replication and modification of naturally occurring substances.
Check Digit Verification of cas no
The CAS Registry Mumber 53608-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53608-93:
(7*5)+(6*3)+(5*6)+(4*0)+(3*8)+(2*9)+(1*3)=128
128 % 10 = 8
So 53608-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O4/c1-3-15-11(13)10(12(14)16-4-2)9-7-5-6-8-9/h5,7,9-10H,3-4,6,8H2,1-2H3
53608-93-8Relevant articles and documents
Lennon et al.
, p. 8426,8438 (1977)
Nickel- and Palladium-Catalyzed Additions of Nucleophiles to Cyclic 1,3-Dienes
Andell, Ove S.,Baeckvall, Jan-E.,Moberg, Christina
, p. 184 - 189 (2007/10/02)
Carbon nucleophiles have been found to add smoothly to 1,3-cyclohexadiene using either a preformed nickel-ligand complex or Ni(0) prepared by in situ reduction of Ni(II) in the presence of a ligand to give 1,2- and 1,4-addition products.Analogous adducts were also obtained from 1,3-cyclopentadiene and 1,3-cyclooctadiene, but the yields were considerably lower.Attempts to add benzenesufinic acid to 1,3-cyclohexadiene using Ni(0) were unsuccessful; this reaction was instead found to be catalyzed by Pd(0)-phosphite complexes.
