58616-95-8 Usage
Uses
Used in Pharmaceutical Industry:
(+/-)-trans-1,2-Cyclopropanedicarboxylic acid is used as a building block for the synthesis of complex molecules, particularly in the development of pharmaceuticals. Its unique structure allows for the creation of novel compounds with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, (+/-)-trans-1,2-Cyclopropanedicarboxylic acid serves as a precursor for the synthesis of various agrochemicals, including pesticides and herbicides. Its versatility in chemical reactions enables the production of effective compounds for agricultural applications.
Used in Organic Synthesis:
(+/-)-trans-1,2-Cyclopropanedicarboxylic acid is utilized as a reagent in organic synthesis, facilitating the formation of new compounds through various chemical reactions. Its presence in the synthesis process can lead to the development of innovative materials and substances.
Used in Chemical Research:
As a valuable chemical in research, (+/-)-trans-1,2-Cyclopropanedicarboxylic acid is employed in studies aimed at understanding its properties, reactivity, and potential applications. Its unique structure and chirality make it an interesting subject for scientific exploration and discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 58616-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,1 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58616-95:
(7*5)+(6*8)+(5*6)+(4*1)+(3*6)+(2*9)+(1*5)=158
158 % 10 = 8
So 58616-95-8 is a valid CAS Registry Number.
58616-95-8Relevant academic research and scientific papers
Potent non-nitrile dipeptidic dipeptidyl peptidase IV inhibitors
Simpkins, Ligaya M.,Bolton, Scott,Pi, Zulan,Sutton, James C.,Kwon, Chet,Zhao, Guohua,Magnin, David R.,Augeri, David J.,Gungor, Timur,Rotella, David P.,Sun, Zhong,Liu, Yajun,Slusarchyk, William S.,Marcinkeviciene, Jovita,Robertson, James G.,Wang, Aiying,Robl, Jeffrey A.,Atwal, Karnail S.,Zahler, Robert L.,Parker, Rex A.,Kirby, Mark S.,Hamann, Lawrence G.
, p. 6476 - 6480 (2008/09/16)
The synthesis and structure-activity relationships of novel dipeptidyl peptidase IV inhibitors replacing the classical cyanopyrrolidine P1 group with other small nitrogen heterocycles are described. A unique potency enhancement was achieved with β-branched natural and unnatural amino acids, particularly adamantylglycines, linked to a (2S,3R)-2,3-methanopyrrolidine based scaffold.
Benzamides derived from 1,2-diaminocyclopropane as novel ligands for human D2 and D3 dopamine receptors
Yang, Donglai,Kefi, Slaheddine,Audinot, Valerie,Millan, Mark-J.,Langlois, Michel
, p. 321 - 327 (2007/10/03)
Benzamides (3a-f) derived from 4-amino-5-chloro-2-methoxybenzoic acid and either cis or trans 1,2-diaminocyclopropane were synthesised and were evaluated in binding assays employing, bovine striatal D2 receptors, recombinant human hD2/sub
