56872-60-7 Usage
Uses
Used in Industrial and Consumer Product Manufacturing:
ETHYL 4-(3,4-DIMETHOXYPHENYL)-4-OXOBUTYRATE is used as a key component in the production of various industrial and consumer products due to its unique chemical properties that contribute to the desired characteristics of the final products.
Used in Research and Development:
This chemical compound is utilized in research and development applications to explore its potential uses and properties in different fields, further expanding its applications and understanding of its capabilities.
Used in Chemical Synthesis:
ETHYL 4-(3,4-DIMETHOXYPHENYL)-4-OXOBUTYRATE is used as a starting material or intermediate in the synthesis of other complex organic compounds, taking advantage of its reactivity and functional groups for further chemical transformations.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL 4-(3,4-DIMETHOXYPHENYL)-4-OXOBUTYRATE may be used as an active pharmaceutical ingredient or as a precursor in the synthesis of drug molecules, leveraging its chemical properties for therapeutic applications.
Used in Cosmetics Industry:
ETHYL 4-(3,4-DIMETHOXYPHENYL)-4-OXOBUTYRATE may also find use in the cosmetics industry, where it can serve as a functional ingredient in formulations, providing specific benefits such as solubility, stability, or other properties that enhance the performance of cosmetic products.
Used in Agricultural Industry:
ETHYL 4-(3,4-DIMETHOXYPHENYL)-4-OXOBUTYRATE could be employed in the agricultural sector, potentially as a component in the development of agrochemicals or as a constituent in formulations that improve crop yield or protect against pests and diseases.
Note: The specific applications mentioned above are hypothetical and based on the general properties of ester compounds. The actual uses of ETHYL 4-(3,4-DIMETHOXYPHENYL)-4-OXOBUTYRATE may vary and would require further research and validation.
Check Digit Verification of cas no
The CAS Registry Mumber 56872-60-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,7 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56872-60:
(7*5)+(6*6)+(5*8)+(4*7)+(3*2)+(2*6)+(1*0)=157
157 % 10 = 7
So 56872-60-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O5/c1-4-19-14(16)8-6-11(15)10-5-7-12(17-2)13(9-10)18-3/h5,7,9H,4,6,8H2,1-3H3
56872-60-7Relevant articles and documents
Synthesis of Annulated Anthracenes, Carbazoles, and Thiophenes Involving Bradsher-Type Cyclodehydration or Cyclization-Reductive-Dehydration Reactions
Rafiq, Settu Muhamad,Sivasakthikumaran, Ramakrishnan,Karunakaran, Jayachandran,Mohanakrishnan, Arasambattu K.
, p. 5099 - 5114 (2015/08/18)
A conventional BF3·OEt2-mediated Bradsher-type cyclodehydration of 2-arylmethyl benzaldehydes in CH2Cl2 at room temperature gave polycyclic aromatic and heteroaromatic compounds. Alternatively, these compounds could be synthesized in better yields from 2-arylmethylbenzoic acids by triflic-acid-mediated cyclization followed by reductive dehydration.
Synthesis and deprotection of 1,3-Dithianes and 1,3-Dithiolanes by polyphosphoric acid
Jin, Yong-Sheng,Zhang, Wei,Zhang, Da-Zhi,Qiao, Li-Ming,Wu, Qiu-Ye,Chen, Hai-Sheng
experimental part, p. 1117 - 1119 (2011/12/16)
A simply, mild and efficient method for the deprotection of 1,3-dithianes and 1,3-dithiolanes to their corresponding carbonyl compounds using a mixture of polyphosphoric acid and acetic acid at 20-45 °C is reported.
Synthesis and characterization of naphth-annelated thiophene analogs
Clement, J. Arul,Mohanakrishnan, Arasambattu K.
experimental part, p. 2340 - 2350 (2010/06/12)
Synthesis of symmetrical and unsymmetrical naphth-annelated thienyl heterocycles has been achieved via thionation of hydroxyketones/diketones using Lawesson's reagent. Photophysical studies of 1,3-disubstituted naphtho[c]thiophene analogs are presented. Electro-oxidative behavior of these naphtha-annelated thiophenes are investigated using cyclic voltammeter.
Studies on non-thiazolidinedione antidiabetic agents. 3. Preparation and biological activity of the metabolites of TAK-559
Imoto, Hiroshi,Matsumoto, Mitsuharu,Odaka, Hiroyuki,Sakamoto, Junichi,Kimura, Hiroyuki,Nonaka, Masami,Kiyota, Yutaka,Momose, Yu
, p. 120 - 124 (2007/10/03)
Preparation and biological activity of the metabolites of the potent antihyperglycemic and antihyperlipidemic agent, (E)-4-{4-[(5-methyl-2-phenyl-1, 3-oxazol-4-yl)methoxy]benzyloxyimino}-4-phenylbutyric acid (TAK-559) (1), were investigated. Metabolites M