856795-95-4 Usage
Description
N-Ethyl-4-bromobenzylamine, also known as N-(4-Bromobenzyl)ethanamine, is an organic compound with a molecular formula of C9H12BrN. It is a derivative of benzylamine, featuring an ethyl group and a bromo substituent on the benzene ring. N-Ethyl-4-bromobenzylamine is a key intermediate in the synthesis of various pharmaceuticals and has potential applications in the development of new therapeutic agents.
Uses
Used in Pharmaceutical Industry:
N-Ethyl-4-bromobenzylamine is used as a key intermediate in the synthesis of 2-Benzoyl-1,2,3,4-tetrahydroisoquinolin-7-ol and 2-Benzoyl-1,2,3,4-tetrahydroisoquinolin-7-yl Sulfamate compounds. These compounds have potential therapeutic applications in the treatment of hormone-dependent diseases, such as breast and prostate cancer, by targeting specific hormonal pathways and receptors involved in the growth and progression of these diseases. The use of N-Ethyl-4-bromobenzylamine in the preparation of these compounds highlights its importance in the development of novel and effective treatments for hormone-dependent conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 856795-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,7,9 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 856795-95:
(8*8)+(7*5)+(6*6)+(5*7)+(4*9)+(3*5)+(2*9)+(1*5)=244
244 % 10 = 4
So 856795-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H12BrN/c1-2-11-7-8-3-5-9(10)6-4-8/h3-6,11H,2,7H2,1H3
856795-95-4Relevant articles and documents
Transformation of N,N-diisopropylarylmethylamines into N-isopropylarylmethylamines with molecular iodine
Ezawa, Masatoshi,Moriyama, Katsuhiko,Togo, Hideo
, p. 6689 - 6692 (2016/02/03)
N,N-Diisopropylarylmethylamines were smoothly converted into the corresponding N-isopropylarylmethylamines by the reaction with molecular iodine in the presence of Na2CO3 in chloroform at 60 °C. Other related tertiary amines were also transformed into the corresponding secondary amines by the reaction with molecular iodine under the same reaction conditions.
