710-43-0 Usage
Description
Diethyl cis-cyclopropane-1,2-dicarboxylate is an organic compound that features a cyclopropane ring with two carboxylate groups attached in a cis configuration. It is a valuable intermediate in organic synthesis due to its unique structural properties and reactivity.
Uses
Used in Synthetic Chemistry:
Diethyl cis-cyclopropane-1,2-dicarboxylate is used as a synthetic intermediate for the preparation of various organic compounds through intermolecular metal-catalyzed carbenoid cyclopropanations. Its unique cyclopropane ring and carboxylate groups make it a versatile building block for creating complex molecular structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Diethyl cis-cyclopropane-1,2-dicarboxylate is used as a key component in the synthesis of certain pharmaceutical compounds. Its ability to participate in cyclopropanation reactions allows for the creation of novel drug candidates with potential therapeutic applications.
Used in Material Science:
Diethyl cis-cyclopropane-1,2-dicarboxylate is also utilized in the development of new materials with specific properties. Its incorporation into polymers and other materials can lead to enhanced mechanical, thermal, or chemical characteristics, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 710-43-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 710-43:
(5*7)+(4*1)+(3*0)+(2*4)+(1*3)=50
50 % 10 = 0
So 710-43-0 is a valid CAS Registry Number.
710-43-0Relevant articles and documents
Cobalt-catalyzed asymmetric cyclopropanation of electron-deficient olefins
Chen, Ying,Ruppel, Joshua V.,Zhang, X. Peter
, p. 12074 - 12075 (2008/03/27)
The cobalt(II) complex of a D2-symmetric chiral porphyrin [Co(1)] is an effective catalyst for asymmetric cyclopropanation of electron-deficient olefins, including α,β-unsaturated esters, amides, ketones, and nitriles. Due to the absence of dimerization of diazo compounds, the catalytic reactions can be performed in one-pot protocol using olefins as the limiting reagent, forming the desired electrophilic cyclopropane derivatives in high yields and selectivities under mild conditions. In most cases, both excellent diastereo- and enantioselectivity were achieved. Copyright
Synthesis of Cyclopropyl Carbocyclic Nucleosides
Csuk, Rene,Scholz, Yvonne von
, p. 10431 - 10442 (2007/10/02)
As representatives of a novel class of carboxylic nucleoside analogues (+/-)-cis-, (-)-cis and (+/-)-trans 9-(2-hydroxymethylcyclopropyl)-adenine (= -methanol) were synthesized from the corresponding dialkyl 1,2-cyclopropane dicarboxylates.
The Synthesis of a Cyclopropane Amino Acid, trans-α-(Carboxycyclopropyl)glycine, found in Ackee Seed
Landor, Stephen R.,Landor, Phyllis, D.,Kalli, Michael
, p. 2921 - 2926 (2007/10/02)
trans-α-(Carboxycyclopropyl)glycine, a constituent of ackee seed (Blighia sapida), has been synthesized via the key intermediate ethyl (E)-4,4-diethoxybut-2-enoate.
