76149-15-0 Usage
Description
4-(2-di-N-propylaminoethyl)indole is a chemical compound belonging to the indole family, characterized by the presence of a propylaminoethyl group attached to the indole nucleus. 4-(2-di-N-propylaminoethyl)indole exhibits unique structural features and potential biological activities, making it a promising candidate for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
4-(2-di-N-propylaminoethyl)indole is used as a pharmaceutical agent for its potential dopamine agonist activity. Its derivatives have been found to modulate dopamine receptors, which play a crucial role in the regulation of various physiological processes, including motor control, cognition, and mood regulation. 4-(2-di-N-propylaminoethyl)indole may be utilized in the development of treatments for neurological disorders such as Parkinson's disease, schizophrenia, and depression.
Used in Drug Delivery Systems:
4-(2-di-N-propylaminoethyl)indole can be employed as a component in drug delivery systems to enhance the bioavailability and therapeutic efficacy of other pharmaceutical agents. Its unique structural features may allow for the development of novel drug carriers, such as nanoparticles or liposomes, that can improve the delivery of drugs to target tissues and cells, thereby increasing their effectiveness and reducing side effects.
Used in Chemical Research:
As a member of the indole family, 4-(2-di-N-propylaminoethyl)indole can be used as a research tool in chemical and biological studies. Its unique structure and potential biological activities make it an interesting subject for investigations into the structure-activity relationships of indole-based compounds, as well as their interactions with various biological targets and pathways.
Used in Agrochemical Industry:
4-(2-di-N-propylaminoethyl)indole may also find applications in the agrochemical industry, where it could be used as a component in the development of novel pesticides or herbicides. Its unique structural features and potential biological activities may enable the design of new compounds with improved efficacy and selectivity, contributing to more sustainable and environmentally friendly agricultural practices.
Check Digit Verification of cas no
The CAS Registry Mumber 76149-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76149-15:
(7*7)+(6*6)+(5*1)+(4*4)+(3*9)+(2*1)+(1*5)=140
140 % 10 = 0
So 76149-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H24N2/c1-3-11-18(12-4-2)13-9-14-6-5-7-16-15(14)8-10-17-16/h5-8,10,17H,3-4,9,11-13H2,1-2H3
76149-15-0Relevant articles and documents
Proposed dopaminergic pharmacophore of lergotrile, pergolide, and related ergot alkaloid derivatives
Cannon,Demopoulos,Long,Flynn,Sharabi
, p. 238 - 240 (1981)
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The development of a short route to the API ropinirole hydrochloride
Yousuf, Zeshan,Richards, Andrew K.,Dwyer, Andrew N.,Linclau, Bruno,Harrowven, David C.
, p. 10532 - 10539 (2015/11/10)
A four-step, three-stage synthesis of the API ropinirole hydrochloride has been developed from a commercially available naphthalene derivative. The new route has half the step-count and twice the overall yield of the current manufacturing process. Key features of the synthesis are a regioselective Birch reduction and an ozonolysis with concomitant ring closure to induce the required ring contraction.
Preparation of alkyl-substituted indoles in the benzene portion. Part 5. Efficient preparative procedure for 4-substituted indole derivatives
Fuji,Muratake,Natsume
, p. 2338 - 2343 (2007/10/02)
An effective and short synthetic method for 4-substituted indole derivatives was developed based on the two sequential reactions, i.e. nucleophilic addition of carbanions to common precursor molecules, 3-(1,3-dioxolan-2-yl)-1-[1(phenylsulfonyl)- and 1-[(4
