87549-50-6 Usage
Uses
Used in Organic Synthesis:
4-(Diethylphosphono)-3-methyl-2-butenenitrile, E/Z mixture is used as a synthetic intermediate in the preparation of various organic compounds. Its unique structure allows it to participate in a wide range of chemical reactions, such as nucleophilic addition, electrophilic substitution, and rearrangement reactions. This versatility makes it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(Diethylphosphono)-3-methyl-2-butenenitrile, E/Z mixture is used as a key intermediate in the synthesis of various drug molecules. Its ability to undergo multiple types of chemical reactions enables the development of complex molecular structures with potential therapeutic properties. 4-(Diethylphosphono)-3-methyl-2-butenenitrile, E/Z mixture can be used to create new drugs or improve the synthesis processes of existing ones, ultimately contributing to the advancement of medicine.
Used in Agrochemical Industry:
4-(Diethylphosphono)-3-methyl-2-butenenitrile, E/Z mixture also finds application in the agrochemical industry, where it serves as a precursor for the synthesis of various agrochemicals, such as pesticides and herbicides. Its unique structure and reactivity allow for the development of new and more effective compounds to protect crops and control pests, thereby contributing to increased agricultural productivity and food security.
Check Digit Verification of cas no
The CAS Registry Mumber 87549-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,4 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87549-50:
(7*8)+(6*7)+(5*5)+(4*4)+(3*9)+(2*5)+(1*0)=176
176 % 10 = 6
So 87549-50-6 is a valid CAS Registry Number.
87549-50-6Relevant academic research and scientific papers
Backbone modification of retinal induces protein-like excited state dynamics in solution
Sovdat, Tina,Bassolino, Giovanni,Liebel, Matz,Schnedermann, Christoph,Fletcher, Stephen P.,Kukura, Philipp
supporting information; experimental part, p. 8318 - 8320 (2012/06/30)
The drastically different reactivity of the retinal chromophore in solution compared to the protein environment is poorly understood. Here, we show that the addition of a methyl group to the C=C backbone of all-trans retinal protonated Schiff base acceler
