443331-14-4 Usage
Uses
Used in Organic Synthesis:
(4-AMINOMETHYL-PHENYL)-CARBAMIC ACID BENZYL ESTER is used as a building block for the synthesis of various biologically active molecules, contributing to the development of new compounds with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-AMINOMETHYL-PHENYL)-CARBAMIC ACID BENZYL ESTER is utilized as a key component in the creation of new drugs and medicines. Its ability to interact with biological targets and receptors positions it as a promising candidate for drug discovery and development.
Used in Medicinal Chemistry:
(4-AMINOMETHYL-PHENYL)-CARBAMIC ACID BENZYL ESTER is employed as a valuable tool for researchers and scientists in medicinal chemistry. Its chemical structure and properties facilitate the exploration of novel therapeutic agents and contribute to advancements in the understanding of molecular interactions within biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 443331-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,3,3 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 443331-14:
(8*4)+(7*4)+(6*3)+(5*3)+(4*3)+(3*1)+(2*1)+(1*4)=114
114 % 10 = 4
So 443331-14-4 is a valid CAS Registry Number.
443331-14-4Relevant academic research and scientific papers
A method for the selective protection of aromatic amines in the presence of aliphatic amines
Perron, Valerie,Abbott, Shaun,Moreau, Nancie,Lee, Devin,Penney, Christopher,Zacharie, Boulos
experimental part, p. 283 - 289 (2009/06/25)
A simple and efficient procedure has been developed for the regioselective protection of aromatic amines in the presence of aliphatic amines. The method is general for the preparation of mono-N-Boc, -N-Cbz, -N-Fmoc or -N-Alloc aromatic amines in high yield without affecting the aliphatic amines. This approach is applicable to substituted (aminoalkyl)aniline compounds with different functionalities and was employed to supply gram quantities of the protected aniline product. Georg Thieme Verlag Stuttgart · New York.
