112856-76-5 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Pentadienoic acid, 5-(2-chlorophenyl)-3-methoxy-, methyl ester, (E,E)is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and functional groups contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Chemistry Research:
In the field of organic chemistry, 2,4-Pentadienoic acid, 5-(2-chlorophenyl)-3-methoxy-, methyl ester, (E,E)serves as a valuable research tool. It is utilized in the study of chemical reactions and mechanisms, providing insights into the behavior of similar organic compounds and aiding in the discovery of novel synthetic pathways.
Used in Biological Studies:
Although the specific mechanisms of action and potential uses are still being explored, 2,4-Pentadienoic acid, 5-(2-chlorophenyl)-3-methoxy-, methyl ester, (E,E)has demonstrated some biological activity. It is used in biological studies to investigate its interactions with biological systems and to assess its potential as a therapeutic agent or a probe for understanding biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 112856-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,5 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112856-76:
(8*1)+(7*1)+(6*2)+(5*8)+(4*5)+(3*6)+(2*7)+(1*6)=125
125 % 10 = 5
So 112856-76-5 is a valid CAS Registry Number.
112856-76-5Relevant academic research and scientific papers
Duc,McGarrity,Meul,Warm
, p. 391 - 394 (1992)
Methyl (E)-4-chloro-3-methoxy-2-butenoate (3a) is inexpensively prepared from methyl 4-chloroacetoacetate using thionyl chloride and methanol on an industrial scale. Many nucleophilic substitution reactions of chloride, which are impossible with the unpro
Amino acid esters, process for the preparation thereof and use thereof
-
, (2008/06/13)
Novel esters of amino acids are proposed of which the alcoholic components are formed from threo-4-alkoxy-5-arylhydroxymethyl-2(5H)-furanones. These esters may be present in the form of racemates, pure diastereomers or enantiomers or in the form of diaste
