60611-95-2 Usage
Description
(E)-ETHYL 4-(4-FLUOROPHENYL)-4-OXOBUT-2-ENOATE, a chemical compound with the molecular formula C12H11FO3, is a yellowish liquid characterized by a fruity odor. It belongs to the ester class and is predominantly utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Due to its flammability and potential hazards, it is crucial to handle and store this compound with caution, avoiding contact with skin, ingestion, and exposure to heat, sparks, or open flames.
Uses
Used in Pharmaceutical Industry:
(E)-ETHYL 4-(4-FLUOROPHENYL)-4-OXOBUT-2-ENOATE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its role in this industry is crucial for the development of new drugs and medications, contributing to the advancement of healthcare and treatment options.
Used in Agrochemical Industry:
In the agrochemical sector, (E)-ETHYL 4-(4-FLUOROPHENYL)-4-OXOBUT-2-ENOATE serves as an intermediate for the production of different agrochemicals. Its application in this industry aids in the development of products that protect crops from pests and diseases, ensuring food security and agricultural productivity.
Overall, (E)-ETHYL 4-(4-FLUOROPHENYL)-4-OXOBUT-2-ENOATE plays a significant role in both the pharmaceutical and agrochemical industries, acting as an essential intermediate in the synthesis of various compounds. However, its potential hazards and flammability necessitate careful handling and storage to prevent accidents and ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 60611-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,1 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60611-95:
(7*6)+(6*0)+(5*6)+(4*1)+(3*1)+(2*9)+(1*5)=102
102 % 10 = 2
So 60611-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H11FO3/c1-2-16-12(15)8-7-11(14)9-3-5-10(13)6-4-9/h3-8H,2H2,1H3/b8-7+
60611-95-2Relevant articles and documents
Synthesis of 1,5-benzodiazepine derivatives using p-toluenesulfonic acid as catalyst
Wang, Shasha,Hu, Lijuan,Cheng, Suyan,Wang, Lanzhi
, p. 419 - 424 (2015/01/30)
A series of substituted ethyl 4-oxo-4-phenylbut-2-enoates were prepared and reacted with substituted o-phenylenediamine, undergone Michael addition reactions and cyclodehydration to provide novel 4-phenyl-2,3-dihydro-1,5-benzodiazepine-2-carboxylate derivatives with excellent yields. The synthetic protocol fulfilled many green-chemical requirements by using simple catalyst p-toluenesulfonic acid as activator and ethanol as solvent at room temperature.
