496790-62-6 Usage
Description
[2-(2-BROMOPHENYL)-2-HYDROXYETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER, also known as Boc-protected 2-aminophenol, is a versatile compound utilized in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in organic synthesis due to its reactivity and is commonly used as a precursor in the preparation of various bioactive molecules and organic compounds, making it an important intermediate in the production of numerous pharmaceuticals and chemical products.
Uses
Used in Pharmaceutical Industry:
[2-(2-BROMOPHENYL)-2-HYDROXYETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER is used as a building block for the synthesis of various pharmaceuticals. Its reactivity and versatility allow for the creation of a wide range of bioactive molecules, contributing to the development of new drugs and treatments.
Used in Agrochemical Industry:
In the agrochemical industry, [2-(2-BROMOPHENYL)-2-HYDROXYETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER is used as a key intermediate in the synthesis of various agrochemicals. Its role in the production of these compounds helps to improve agricultural productivity and protect crops from pests and diseases.
Used in Organic Synthesis:
[2-(2-BROMOPHENYL)-2-HYDROXYETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER is used as a precursor in organic synthesis for the preparation of various organic compounds. Its reactivity and structural properties make it a valuable component in the development of new chemical products and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 496790-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,7,9 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 496790-62:
(8*4)+(7*9)+(6*6)+(5*7)+(4*9)+(3*0)+(2*6)+(1*2)=216
216 % 10 = 6
So 496790-62-6 is a valid CAS Registry Number.
496790-62-6Relevant articles and documents
Direct catalytic synthesis of unprotected 2-amino-1-phenylethanols from alkenes by using iron(II) phthalocyanine
Legnani, Luca,Morandi, Bill
supporting information, p. 2248 - 2251 (2016/02/18)
Aryl-substituted amino alcohols are privileged scaffolds in medicinal chemistry and natural products. Herein, we report that an exceptionally simple and inexpensive FeII complex efficiently catalyzes the direct transformation of simple alkenes into unprotected amino alcohols in good yield and perfect regioselectivity. This new catalytic method was applied in the expedient synthesis of bioactive molecules and could be extended to aminoetherification.
