58246-00-7 Usage
Description
(2-Acetyl-1,2-dihydroisoquinolin-1-yl)acetic acid is a chemical compound derived from isoquinoline, a heterocyclic aromatic organic compound. It has potential therapeutic applications and has been studied for its potential use as an analgesic, anti-inflammatory agent, and histamine H3 receptor antagonist. Additionally, it has been explored for its potential role in modulating neurotransmitter levels in the brain, particularly dopamine and serotonin.
Used in Pharmaceutical Industry:
(2-Acetyl-1,2-dihydroisoquinolin-1-yl)acetic acid is used as an analgesic and anti-inflammatory agent for its potential to alleviate pain and reduce inflammation. It is also used as a histamine H3 receptor antagonist, which may have therapeutic benefits in various conditions.
Used in Neurotransmitter Modulation:
(2-Acetyl-1,2-dihydroisoquinolin-1-yl)acetic acid is used as a modulator of neurotransmitter levels in the brain, particularly dopamine and serotonin, which may have potential applications in treating neurological and psychiatric disorders.
Further research is needed to fully understand the pharmacological properties and potential medical applications of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 58246-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,4 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58246-00:
(7*5)+(6*8)+(5*2)+(4*4)+(3*6)+(2*0)+(1*0)=127
127 % 10 = 7
So 58246-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO3/c1-9(15)14-7-6-10-4-2-3-5-11(10)12(14)8-13(16)17/h2-7,12H,8H2,1H3,(H,16,17)
58246-00-7Relevant articles and documents
Studies on Quinoline and Isoquinoline Derivatives. VII. Addition Reactions of Acetic Anhydride and Active Methylene Compounds to the Carbon-Nitrogen Double Bond of the Isoquinoline Ring
Yamanaka, Hiroshi,Shiraishi, Takayuki,Sakamoto, Takao
, p. 1056 - 1062 (2007/10/02)
Acetic anhydride reacted with isoquinoline (IV) itself under reflux to give an addition product, whereas quinoline did not react with acetic anhydride under the same conditions.The structure of the product was determined to be 2-acetyl-1,2-dihydroisoquino
