387356-94-7 Usage
Uses
Used in Chemical Research:
(E)-Ethyl 2-(4-Methoxy-3-(3-Methoxypropoxy)benzylidene)-3-Methylbutanoate is used as a research compound for studying its chemical properties and potential applications in various fields. Its unique structure allows for investigation into its reactivity and behavior in different chemical reactions.
Used in Industrial Applications:
In the chemical industry, (E)-Ethyl 2-(4-Methoxy-3-(3-Methoxypropoxy)benzylidene)-3-Methylbutanoate may be employed as an intermediate in the synthesis of other complex organic compounds or as a component in the formulation of various products. Its specific properties, such as solubility and stability, can be advantageous in these applications.
Used in Pharmaceutical Development:
(E)-Ethyl 2-(4-Methoxy-3-(3-Methoxypropoxy)benzylidene)-3-Methylbutanoate could be utilized in the development of pharmaceuticals, potentially serving as a precursor to active pharmaceutical ingredients or as a component in drug delivery systems. Its unique structure may offer specific advantages in the design and synthesis of new medicinal compounds.
Used in Material Science:
In the field of material science, (E)-Ethyl 2-(4-Methoxy-3-(3-Methoxypropoxy)benzylidene)-3-Methylbutanoate may be explored for its potential use in the development of new materials with specialized properties. Its chemical structure could contribute to the creation of materials with unique characteristics, such as improved stability or specific interactions with other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 387356-94-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,7,3,5 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 387356-94:
(8*3)+(7*8)+(6*7)+(5*3)+(4*5)+(3*6)+(2*9)+(1*4)=197
197 % 10 = 7
So 387356-94-7 is a valid CAS Registry Number.
387356-94-7Relevant articles and documents
Asymmetric hydrogenation of α,β-unsaturated carboxylic esters with chiral iridium N,P ligand complexes
Woodmansee, David H.,Mueller, Marc-Andre,Troendlin, Lars,Hoermann, Esther,Pfaltz, Andreas
supporting information, p. 13780 - 13786 (2013/01/15)
Enantioselective conjugate reduction of a wide range of α,β-unsaturated carboxylic esters was achieved using chiral Ir N,P complexes as hydrogenation catalysts. Depending on the substitution pattern of the substrate, different ligands perform best. α,β-Unsaturated carboxylic esters substituted at the α position are less problematic substrates than originally anticipated and in some cases α-substituted substrates actually reacted with higher enantioselectivity than their β-substituted analogues. The resulting saturated esters with a stereogenic center in the α or β position were obtained in high enantiomeric purity. Copyright
Acid promoted CIDT for the deracemization of dihydrocinnamic aldehydes with Betti's base
Rosini, Goffredo,Paolucci, Claudio,Boschi, Francesca,Marotta, Emanuela,Righi, Paolo,Tozzi, Francesco
supporting information; experimental part, p. 1747 - 1757 (2011/02/28)
Racemic α-epimerizable and unfunctionalized aldehydes have been converted into enantiomerically enriched mixtures through a sequence of (i) a conversion into the diastereoisomeric 3-substituted 1-phenyl-2,3-dihydro-1H- naphtho[1,2-e][1,3]oxazines by reaction with the (R)- or (S)-1-(α- aminobenzyl)-2-naphthol (Betti's base), (ii) an acid promoted crystallization-induced diastereoisomer transformation (CIDT), and (iii) a clean cleavage of the dihydro-1,3-naphthoxazinic ring of the enriched diastereoisomer, easily collected by filtration, allowing the recovery of the enantiomerically enriched aldehydes and the chiral auxiliary.
