104807-65-0 Usage
Uses
Used in Organic Synthesis:
Ethyl 2-iodo-5-methoxybenzoate is used as a building block in organic synthesis for the creation of more complex molecules. Its unique structure allows for various chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Ethyl 2-iodo-5-methoxybenzoate is used as a starting material or intermediate in the development of new drugs. Its unique properties and reactivity make it a promising candidate for the synthesis of novel therapeutic agents.
Used in Biological and Pharmacological Studies:
Ethyl 2-iodo-5-methoxybenzoate is also used in biological and pharmacological research to explore its potential activities and applications. Although its precise uses in these fields are still being investigated, its unique structure and properties suggest that it may have potential as a therapeutic agent or a tool for understanding biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 104807-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,0 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104807-65:
(8*1)+(7*0)+(6*4)+(5*8)+(4*0)+(3*7)+(2*6)+(1*5)=110
110 % 10 = 0
So 104807-65-0 is a valid CAS Registry Number.
104807-65-0Relevant articles and documents
One-Pot C-H Arylation/Lactamization Cascade Reaction of Free Benzylamines
Chand-Thakuri, Pratibha,Landge, Vinod G.,Kapoor, Mohit,Young, Michael C.
, p. 6626 - 6644 (2020/07/14)
An efficient method has been developed for the synthesis of seven-membered biaryl lactams involving Pd-catalyzed, native amine-directed, ortho-arylation of benzylamines followed by in situ lactamization. This cascade sequence is enabled by the use of 2-iodobenzoates, which facilitates C-H arylation from the free amine under conditions that typically require an improved directing group approach. This reaction is characterized by a broad substrate scope with good functional group tolerance. The need for an ester versus carboxylic acid-functionalized coupling partner is also explored, as is the potential for synthesizing eight-membered biaryl lactams. Various applications are also investigated, including access to the aza-brassinolide core.
