1211596-98-3 Usage
Uses
Used in Pharmaceutical Research:
1H-Azepine-4-carboxylic acid, hexahydro-, methyl ester is used as a building block in pharmaceutical research for the synthesis of various bioactive compounds. Its unique structure and properties make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 1H-Azepine-4-carboxylic acid, hexahydro-, methyl ester is utilized as an intermediate compound. Its presence in the synthesis process contributes to the creation of pharmaceuticals and other fine chemicals, highlighting its importance in the production of these specialized products.
Check Digit Verification of cas no
The CAS Registry Mumber 1211596-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,5,9 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1211596-98:
(9*1)+(8*2)+(7*1)+(6*1)+(5*5)+(4*9)+(3*6)+(2*9)+(1*8)=143
143 % 10 = 3
So 1211596-98-3 is a valid CAS Registry Number.
1211596-98-3Relevant articles and documents
The 2-(2-Azidoethyl)cycloalkanone strategy for bridged amides and medium-sized cyclic amine derivatives in the Aubé-Schmidt reaction
Macleod, Fraser,Lang, Stuart,Murphy, John A.
supporting information; experimental part, p. 529 - 534 (2010/10/02)
2-(2-Azidoethyl)cycloalkanones afford bridged lactams in the Aubé-Schmidt reaction, sometimes in excellent yield, and solvolysis yields derivatives of medium-ring amines. Attempts to divert the Schmidt reaction with an arene-mediated fragmentation of the normal Schmidt intermediate have led to an initial example. Georg Thieme Verlag Stuttgart.
