35304-87-1 Usage
Description
(E)-5-(phenylmethylene)furan-2(5H)-one, with the molecular formula C12H8O2, is a yellow crystalline solid that is recognized for its aromatic and fruity odor. This chemical compound is valued for its unique structure and properties, which make it a versatile building block in the creation of new and diverse compounds with potential commercial and scientific utility.
Uses
Used in Pharmaceutical and Agrochemical Industries:
(E)-5-(phenylmethylene)furan-2(5H)-one is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its distinctive structure allows for the development of novel compounds with potential applications in these fields.
Used in Research and Development:
(E)-5-(phenylmethylene)furan-2(5H)-one is also employed in research and development, where it is studied for its potential biological activities and implications in drug development. The exploration of its properties and interactions with other molecules contributes to the advancement of chemistry and pharmacology.
Used in Chemical Synthesis:
(E)-5-(phenylmethylene)furan-2(5H)-one serves as a valuable building block in chemical synthesis, enabling the creation of a wide range of compounds with diverse applications across various industries. Its unique properties make it a promising candidate for the development of new products with commercial and scientific potential.
Check Digit Verification of cas no
The CAS Registry Mumber 35304-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,0 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35304-87:
(7*3)+(6*5)+(5*3)+(4*0)+(3*4)+(2*8)+(1*7)=101
101 % 10 = 1
So 35304-87-1 is a valid CAS Registry Number.
35304-87-1Relevant articles and documents
Ring-Closing Metathesis Reactions of Acyloxysulfones: Synthesis of γ-Alkylidene Butenolides
Phan, Iris T.,Gilbert, Garrett J.,O'Neil, Gregory W.
, p. 1867 - 1871 (2015/08/06)
An acyloxysulfone ring-closing metathesis/sulfone elimination sequence has been developed for the preparation of various γ-alkylidene butenolides. The elimination is proposed to proceed via an E1cb mechanism leading to (Z)-γ-alkylidene butenolides as the major products.
THE SERIES OF SUBSTITUTED BUTANOLIDES AND BUTENOLIDES. IV. 4-ARYLIDENE(HETEROARYLIDENE)-2-BUTENOLIDES
Sorotskaya, L.N.,Badovskaya, L.A.,Kaklyugina, T.Ya.,Belenkii, L.A.,Ignatenko, A.V.,et al.
, p. 159 - 165 (2007/10/02)
A larger number of 4-arylidene- and 4-heteroarylidene-2-butenolides were obtained by the reaction of 2-butenolide with aromatic and heteroaromatic aldehydes in the presence of piperidine.
