114736-26-4 Usage
Description
(E)-4,4-dimethoxy-but-2-enoic acid ethyl ester, also known as ethyl (E)-4,4-dimethoxy-2-butenoate, is a chemical compound with the molecular formula C9H14O5. It is an ester formed from the condensation of ethyl alcohol and (E)-4,4-dimethoxy-but-2-enoic acid. (E)-4,4-dimethoxy-but-2-enoic acid ethyl ester is characterized by its potential biological activities, including anti-inflammatory and anti-proliferative properties, making it a promising candidate for various applications in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Industry:
(E)-4,4-dimethoxy-but-2-enoic acid ethyl ester is used as a synthetic intermediate for the production of various pharmaceuticals. Its anti-inflammatory and anti-proliferative properties contribute to the development of drugs targeting inflammation and cell proliferation-related diseases.
Used in Agrochemical Industry:
In the agrochemical industry, (E)-4,4-dimethoxy-but-2-enoic acid ethyl ester serves as a synthetic intermediate for the creation of compounds with potential applications in pest control and crop protection. Its reactivity and structural features allow for the synthesis of more complex molecules with specific pesticidal properties.
Used in Organic Chemistry:
(E)-4,4-dimethoxy-but-2-enoic acid ethyl ester is used as a valuable building block in organic chemistry for the synthesis of more complex organic molecules. Its structure and reactivity make it an essential component in the development of advanced materials and compounds with diverse applications.
Used in Fine Chemicals Industry:
(E)-4,4-dimethoxy-but-2-enoic acid ethyl ester is also utilized in the fine chemicals industry, where it is employed as a synthetic intermediate for the production of specialty chemicals with specific applications in various fields, such as fragrances, dyes, and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 114736-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114736-26:
(8*1)+(7*1)+(6*4)+(5*7)+(4*3)+(3*6)+(2*2)+(1*6)=114
114 % 10 = 4
So 114736-26-4 is a valid CAS Registry Number.
114736-26-4Relevant articles and documents
Organocatalyzed Michael-Henry reactions: Enantioselective synthesis of cyclopentanecarbaldehydes via the dienamine organocatalysis of a succinaldehyde surrogate
Hong, Bor-Cherng,Chen, Po-Yuan,Kotame, Prakash,Lu, Pei-Ying,Lee, Gene-Hsiang,Liao, Ju-Hsiou
supporting information; experimental part, p. 7790 - 7792 (2012/09/22)
Asymmetric formal [3+2] cycloadditions of 4-hydroxybut-2-enal, a succinaldehyde surrogate, and nitroalkenes with an organocatalyst provided cyclopentanecarbaldehydes containing four consecutive stereogenic centers with excellent enantioselectivities.
IMIDAZOPYRIDAZINES FOR USE AS PROTEIN KINASE INHIBITORS
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Page/Page column 139-140, (2009/06/27)
There is provided compounds of formula (I): wherein Z, M, R1, X, R3, R4 and R5 have meanings given in the description, an pharmaceutically-acceptable esters, amides, solvates or salts thereof, which compounds are useful in the treatment of diseases in which inhibition of a protei kinase (e.g. a PIM family kinase or PI3-K) is desired and/or required, an particularly in the treatment of cancer.
SYNTHESE STEREOSELECTIVE DU DECADIENE-2(E), 4(Z)OATE D'ETHYLE. A PARTIR D'UN MONOACETAL DU GLYOXAL
Stambouli, A.,Amouroux, R.,Chastrette, M.
, p. 5301 - 5302 (2007/10/02)
The glyoxal monoacetal 2, now readily available in bulk quantity, is a very useful synthon for the dienes-1,3 synthesis, as illustrated in the stereoselective preparation of ethyl 2E,4Z-decadienoate using two Wittig-type olefination reactions.
