3403-45-0 Usage
Uses
Used in Pharmaceutical Industry:
Tert-butyl (4-methyloxazol-5-yl)carbamate is used as a reagent in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the creation of new compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, tert-butyl (4-methyloxazol-5-yl)carbamate is used as a reagent for the synthesis of agrochemicals. Its ability to form new compounds makes it valuable in developing novel products for agricultural use.
Used as Antifungal and Antibacterial Agent:
Tert-butyl (4-methyloxazol-5-yl)carbamate exhibits antifungal and antibacterial properties, making it a potentially valuable ingredient in the development of novel therapeutic agents. Its ability to inhibit the growth of harmful microorganisms can contribute to the creation of new treatments for various infections.
Safety Precautions:
It is important to handle tert-butyl (4-methyloxazol-5-yl)carbamate with caution, as it may pose hazards to human health and the environment. Proper safety precautions should be followed when working with tert-butyl (4-methyloxazol-5-yl)carbamate to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 3403-45-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3403-45:
(6*3)+(5*4)+(4*0)+(3*3)+(2*4)+(1*5)=60
60 % 10 = 0
So 3403-45-0 is a valid CAS Registry Number.
3403-45-0Relevant academic research and scientific papers
Formation of 6-Azaindoles by Intramolecular Diels-Alder Reaction of Oxazoles and Total Synthesis of Marinoquinoline A
Jhaveri, Dishit P.,Osano, Mana,Wipf, Peter
supporting information, p. 2215 - 2219 (2020/04/09)
A new variant of the intramolecular Diels-Alder oxazole (IMDAO) cycloaddition that provides direct access to 6-azaindoles was developed. The IMDAO reaction was applied in a total synthesis of the aminophenylpyrrole-derived alkaloid marinoquinoline A, also
