56872-60-7 Usage
General Description
ETHYL 4-(3,4-DIMETHOXYPHENYL)-4-OXOBUTYRATE is a chemical compound with the molecular formula C13H16O5. It is a member of the ester class of organic compounds, and is specifically classified as an oxo ester. This chemical is commonly used in the manufacturing of various industrial and consumer products, as well as in research and development applications. It is often utilized for its unique chemical properties, which make it suitable for use in a variety of different processes and products.ETHYL 4-(3,4-DIMETHOXYPHENYL)-4-OXOBUTYRATE is also known by its chemical name, and is readily available from a variety of chemical suppliers for use in commercial and industrial applications.
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 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.
