627040-50-0 Usage
Description
N-(3-(4-bromophenoxy)propyl)-N-butylbutan-1-amine is a chemical compound characterized by a butylbutan-1-amine backbone with a 4-bromophenoxypropyl group attached to one of the amine groups. As an amine, it features a basic nitrogen atom with a lone pair, which may contribute to its reactivity and potential applications in various fields.
Uses
Used in Pharmaceutical Research and Development:
N-(3-(4-bromophenoxy)propyl)-N-butylbutan-1-amine is utilized as a compound in pharmaceutical research and development due to its unique structure and potential interactions with biological systems. Its amine group and bromophenoxypropyl moiety may allow it to form complexes or participate in chemical reactions that are relevant to drug discovery and design.
Used as an Intermediate in Organic Synthesis:
This specific compound may also serve as an intermediate in the synthesis of other organic compounds. Its structural features could be exploited in the creation of more complex molecules or in the modification of existing ones, broadening its utility in organic chemistry and related industries.
Given the compound's classification and structural attributes, further experimental study and analysis would be required to fully determine its uses and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 627040-50-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,7,0,4 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 627040-50:
(8*6)+(7*2)+(6*7)+(5*0)+(4*4)+(3*0)+(2*5)+(1*0)=130
130 % 10 = 0
So 627040-50-0 is a valid CAS Registry Number.
627040-50-0Relevant articles and documents
Convergent synthesis of dronedarone, an antiarrhythmic agent
Okitsu, Takashi,Ogasahara, Mizuki,Wada, Akimori
, p. 1149 - 1153 (2016/08/11)
We have developed a convergent synthesis of dronedarone, an antiarrhythmic agent. The key steps of the process are the construction of a benzofuran skeleton by iodocyclization and the carbonylative Suzuki-Miyaura cross-coupling for biaryl ketone formation. This synthetic route required only eight steps from 2-amino-4-nitrophenol in 23% overall yield.
PROCESS FOR THE PREPARATION OF 3-AROYL-5-AMINOBENZOFURAN DERIVATIVES
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Page/Page column 42, (2012/05/31)
The present invention relates to a process for the preparation of 3-aroyl -5- aminobenzofuran derivatives useful as antiarrhythmic drugs which avoids the use of nitro intermediates.
