30684-06-1 Usage
Description
4-Phenylbutylamine hydrochloride is a hydrochloride salt form of the compound 4-Phenylbutylamine, a monoamine compound that functions as a selective norepinephrine releasing agent. It is often utilized as a research chemical and in pharmaceutical applications, with the capacity to elevate norepinephrine levels in the brain, leading to stimulant and mood-enhancing effects.
Used in Pharmaceutical Industry:
4-Phenylbutylamine hydrochloride is used as a research chemical for its potential role in the development of treatments for conditions such as attention deficit hyperactivity disorder (ADHD) and depression. Its ability to increase norepinephrine levels in the brain suggests its potential use in modulating mood and cognitive function.
Used in Research Applications:
4-Phenylbutylamine hydrochloride is used as a research tool to study the effects of norepinephrine on the brain and its implications in various neurological and psychological conditions. This helps in understanding the underlying mechanisms and potential therapeutic uses of the compound.
It is crucial to handle 4-Phenylbutylamine hydrochloride with care and to use it only for its intended purposes under the guidance of a qualified professional, as its safety and efficacy for specific uses are still being studied.
Check Digit Verification of cas no
The CAS Registry Mumber 30684-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,8 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30684-06:
(7*3)+(6*0)+(5*6)+(4*8)+(3*4)+(2*0)+(1*6)=101
101 % 10 = 1
So 30684-06-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H15N.CH4/c11-9-5-4-8-10-6-2-1-3-7-10;/h1-3,6-7H,4-5,8-9,11H2;1H4
30684-06-1Relevant articles and documents
Reduction deuteration method of unsaturated organic compound containing carbon-carbon triple bond and/or carbon-nitrogen triple bond (by machine translation)
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Paragraph 0172-0175, (2019/10/15)
A single electron transfer reaction of an alkali metal medium is applied to reduction of a carbon-carbon triple bond or a carbon-nitrogen triple bond, and an alkyne and a nitrile compound can be respectively converted into deuterated olefin (or alkane) an
Mild N-deacylation of secondary amides by alkylation with organocerium reagents
Wang, Ai-E.,Chang, Zong,Liu, Yong-Peng,Huang, Pei-Qiang
supporting information, p. 1055 - 1058 (2015/09/01)
Secondary amides are a class of highly stable compounds serving as versatile starting materials, intermediates and directing groups (amido groups) in organic synthesis. The direct deacylation of secondary amides to release amines is an important transformation in organic synthesis. Here, we report a protocol for the deacylation of secondary amides and isolation of amines. The method is based on the activation of amides with Tf2O, followed by addition of organocerium reagents, and acidic work-up. The reaction proceeded under mild conditions and afforded the corresponding amines, isolated as their hydrochloride salts, in good yields. In combination with the C-H activation functionalization methodology, the method is applicable to the functionalization of aniline as well as conversion of carboxylic derivatives to functionalized ketones.
