133101-17-4 Usage
Uses
Used in Pharmaceutical Industry:
(2-carbethoxy-4-methoxyphenyl)-acetonitrile is used as a building block for the synthesis of various pharmaceuticals, leveraging its chemical structure to create novel compounds with specific biological activities. Its versatility in molecular synthesis contributes to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical field, (2-carbethoxy-4-methoxyphenyl)-acetonitrile serves as a key intermediate for the synthesis of various agrochemicals. Its role in creating new compounds with targeted biological effects is essential for developing innovative solutions for crop protection and other agricultural applications.
Used in Medicinal Chemistry Research:
(2-carbethoxy-4-methoxyphenyl)-acetonitrile is utilized as a starting material in medicinal chemistry research, where it is further modified and derivatized to explore its potential in creating new drugs. Its unique properties make it a valuable tool for scientists working on drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 133101-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,1,0 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133101-17:
(8*1)+(7*3)+(6*3)+(5*1)+(4*0)+(3*1)+(2*1)+(1*7)=64
64 % 10 = 4
So 133101-17-4 is a valid CAS Registry Number.
133101-17-4Relevant academic research and scientific papers
Meng, Xiangtai,Chen, Dengfeng,Liu, Rui,Jiang, Ping,Huang, Shenlin
, p. 10852 - 10860 (2021)
A novel synthesis of 2-(cyanomethyl)benzoic esters from indanone derivatives has been established. This reaction proceeds via a deprotonation of alcohols with a chemical base, followed by a nucleophilic addition to indanones and Beckmann fragmentation. In addition, this reaction could also work under electrochemical conditions, and no external chemical bases were needed. This mild method offers a novel strategy for the late-stage functionalization of various natural alcohols.
Preparation of Anthraquinones from 10-Hydroxy-9-anthracenecarbonitriles Obtained from a Novel Aryne Annulation Reaction
Bhawal, Baburao M.,Khanapure, Subhash P.,Zhang, Hongming,Biehl, Edward R.
, p. 2846 - 2849 (2007/10/02)
A new method for brief regioselective synthesis of anthraquinones via the reaction of anions of ethyl cyanoacetate or the anions of 2-(carbethoxyaryl)acetonitriles with arynes is described.
