60509-38-8 Usage
Description
N-(2-Bromophenylmethyl)butylamine is a chemical compound with the molecular formula C11H16BrN. It is a substituted phenethylamine derivative, characterized by a butylamine chain with a bromophenylmethyl group attached to the nitrogen atom. N-(2-Bromophenylmethyl)butylamine may hold potential in medicinal chemistry, particularly for the development of pharmaceuticals or drug discovery. However, further research is required to fully explore its properties and potential applications. Due to its potential hazardous nature, it is crucial to handle this chemical with care and follow proper safety protocols.
Uses
Used in Pharmaceutical Development:
N-(2-Bromophenylmethyl)butylamine is used as a chemical intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure may contribute to the development of new medications with specific therapeutic effects.
Used in Drug Discovery:
In the field of drug discovery, N-(2-Bromophenylmethyl)butylamine serves as a potential candidate for the creation of novel compounds with medicinal properties. Its structural features could be leveraged to design drugs targeting specific biological pathways or receptors.
Used in Medicinal Chemistry Research:
N-(2-Bromophenylmethyl)butylamine is utilized in medicinal chemistry research to study the structure-activity relationships of phenethylamine derivatives. This can aid in understanding how modifications to the molecule affect its biological activity and potential therapeutic uses.
Check Digit Verification of cas no
The CAS Registry Mumber 60509-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,0 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60509-38:
(7*6)+(6*0)+(5*5)+(4*0)+(3*9)+(2*3)+(1*8)=108
108 % 10 = 8
So 60509-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16BrN/c1-2-3-8-13-9-10-6-4-5-7-11(10)12/h4-7,13H,2-3,8-9H2,1H3
60509-38-8Relevant articles and documents
Pd-Catalyzed Selective Synthesis of Cyclic Sulfonamides and Sulfinamides Using K2S2O5 as a Sulfur Dioxide Surrogate
Konishi, Hideyuki,Tanaka, Hiromichi,Manabe, Kei
, p. 1578 - 1581 (2017/04/13)
A variety of cyclic sulfonamides and sulfinamides could be selectively synthesized under Pd catalysis using haloarenes bearing amino groups and a sulfur dioxide (SO2) surrogate. The amount of base was key in determining the selectivity. Mechanistic studies revealed that sulfinamides were initially formed via an unprecedented formal insertion of sulfur monoxide and were oxidized to sulfonamides in the presence of an iodide ion and DMSO.
Synthesis of symmetric 1,4-diamino-2-butynes via a Cu(I)-catalyzed one-pot A3-coupling/decarboxylative coupling of a propiolic acid, an aldehyde, and an amine
Feng, Huangdi,Ermolat'ev, Denis S.,Song, Gonghua,Van Der Eycken, Erik V.
experimental part, p. 5149 - 5154 (2012/07/14)
A novel microwave-assisted approach for the one-pot Cu(I)-catalyzed A 3-coupling/decarboxylative coupling (PA2-coupling) of a propiolic acid, an aldehyde, and an amine, resulting in the formation of diversely substituted 1,4-diamino-2-butynes,is described. It is noteworthy that this new multicomponent coupling provides an efficient access to introduce alkyl and aryl group at the 1,4-position of the 1,4-diamino-2-butynes.
