1270498-27-5 Usage
General Description
1H-Azepine-1-carboxylic acid, 3-amino hexahydro, phenylmethyl ester is a chemical compound with the molecular formula C14H21NO2. It is an ester derivative of 1H-azepine-1-carboxylic acid, and its structure includes a six-membered ring with an amino group and a phenylmethyl ester group attached. 1H-Azepine-1-carboxylic acid, 3-aMinohexahydro-, phenylMethyl ester is often used in organic synthesis and pharmaceutical research due to its potential biological and pharmacological activities. It may also be used as a building block in the synthesis of various organic compounds, and its properties and reactions are of interest to chemists and researchers in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1270498-27-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,0,4,9 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1270498-27:
(9*1)+(8*2)+(7*7)+(6*0)+(5*4)+(4*9)+(3*8)+(2*2)+(1*7)=165
165 % 10 = 5
So 1270498-27-5 is a valid CAS Registry Number.
1270498-27-5Relevant articles and documents
Synthesis of β-Diamine Building Blocks by Photocatalytic Hydroamination of Enecarbamates with Amines, Ammonia and N?H Heterocycles
Francis, Daniel,Nelson, Adam,Marsden, Stephen P.
, p. 14861 - 14865 (2020/10/12)
3-Amino-substituted saturated nitrogen heterocycles are an important subclass of β-diamines, appearing in a number of clinical agents. Herein, we report a unified approach to these products based upon the regioselective photoredox-mediated hydroamination of enecarbamates. The amine coupling partner can encompass diverse amine types under a single set of reaction conditions, including primary alkyl amines, ammonia, aryl and heteroaryl amines, and N?H heterocycles. The method enables the synthesis of a wide range of pharmaceutically relevant building blocks.