96914-67-9 Usage
Uses
Used in Pharmaceutical Industry:
(E)-2-CYANO-5-METHYL-HEX-2-ENOIC ACID METHYL ESTER is used as a starting material for the synthesis of various pharmaceutical compounds due to its unique reactivity and structural properties. Its ability to be modified and incorporated into more complex molecules makes it a promising candidate for the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, (E)-2-CYANO-5-METHYL-HEX-2-ENOIC ACID METHYL ESTER is utilized as a building block for the creation of pesticides, herbicides, and other agricultural chemicals. Its structural diversity allows for the development of targeted and effective products that can enhance crop protection and yield.
Used in Analytical Chemistry:
(E)-2-CYANO-5-METHYL-HEX-2-ENOIC ACID METHYL ESTER is used as a reference standard for the identification and quantification of similar compounds in analytical chemistry. Its distinct properties make it an ideal tool for researchers and scientists to ensure accurate and reliable results in their experiments and analyses.
Used in Scientific Research:
This versatile chemical is also employed in scientific research for exploring new reactions, understanding mechanisms, and developing novel methodologies in organic chemistry. Its unique structure and reactivity provide a foundation for the discovery of new chemical processes and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 96914-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,9,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96914-67:
(7*9)+(6*6)+(5*9)+(4*1)+(3*4)+(2*6)+(1*7)=179
179 % 10 = 9
So 96914-67-9 is a valid CAS Registry Number.
96914-67-9Relevant academic research and scientific papers
Novel cyclopropyl β-amino acid analogues of pregabalin and gabapentin that target the α2-δ protein
Schwarz, Jacob B.,Gibbons, Sian E.,Graham, Shelley R.,Colbry, Norman L.,Guzzo, Peter R.,Le, Van-Duc,Vartanian, Mark G.,Kinsora, Jack J.,Lotarski, Susan M.,Li, Zheng,Dickerson, Melvin R.,Su, Ti-Zhi,Weber, Mark L.,El-Kattan, Ayman,Thorpe, Andrew J.,Donevan, Sean D.,Taylor, Charles P.,Wustrow, David J.
, p. 3026 - 3035 (2007/10/03)
As part of a program aimed at generating compounds with affinity for the α2-δ subunit of voltage-gated calcium channels, several novel β-amino acids were prepared using an efficient nitroalkane-mediated cyclopropanation as a key step. Depending
Cyclopropyl beta-amino acid derivatives
-
, (2008/06/13)
This invention relates to novel cyclopropyl β-amino acids derivatives of the formula wherein R1 through R4 are defined as in the specification, pharmaceutical compositions containing them and their use for the treatment of various ce
Intramolecular Ene Reactions, III. - Diastereoselective Formation of Cyclohexanes by Intramolecular Ene Reactions of 1,7-Dienes
Tietze, Lutz F.,Beifuss, Uwe
, p. 321 - 330 (2007/10/02)
The 1,7-dienes 3a-c with a double-activated enophile moiety undergo thermal and zinc bromide catalyzed intramolecular ene reactions leading to trans-1,2-disubstituted cyclohexanes 4a-c in up to 89 percent yield, highly diastereoselectively.The synthesis of cyclohexanes from 1,7-dienes has not been feasible so far in a selective way and with good yields.Reaction of 3d, 3e, and 3f gives mixtures of intramolecular hetero Diels-Alder adducts, ene and tandem ene products.The 1,7-dienes 3 are obtained by Knoevenagel condensation of 7-methyl-6-octenal (2) with acyclic 1,3-dicarbonyl and analogous compounds 1.
