1359987-62-4 Usage
Molecular structure
A molecule with a 3,4-dihydroisoquinoline core, a methyl group at the 1-position, and a tert-butyl group at the 2-position. It also has two carboxylate groups at the 1,2-position.
Receptor selectivity
Talsaclidine is a selective M1 muscarinic receptor agonist, meaning it specifically targets the M1 subtype of muscarinic acetylcholine receptors in the brain.
Therapeutic potential
Talsaclidine has been studied for its potential therapeutic effects in the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's.
Mechanism of action
Talsaclidine enhances cognitive function and motor control by targeting the M1 muscarinic receptors in the brain.
Preclinical studies
Talsaclidine has shown promise in preclinical studies for its ability to enhance cognitive function and motor control.
Further research needed
Further research and clinical trials are needed to fully understand the potential benefits and any potential side effects of Talsaclidine.
Check Digit Verification of cas no
The CAS Registry Mumber 1359987-62-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,9,9,8 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1359987-62:
(9*1)+(8*3)+(7*5)+(6*9)+(5*9)+(4*8)+(3*7)+(2*6)+(1*2)=234
234 % 10 = 4
So 1359987-62-4 is a valid CAS Registry Number.
1359987-62-4Relevant academic research and scientific papers
A soluble iron(ii)-phthalocyanine-catalyzed intramolecular C(sp3)-H amination with alkyl azides
You, Tingjie,Zeng, Si-Hao,Fan, Jianqiang,Wu, Liangliang,Kang, Fangyuan,Liu, Yungen,Che, Chi-Ming
, p. 10711 - 10714 (2021/10/20)
Herein, we describe a soluble iron(ii)-phthalocyanine, [FeII(tBu4Pc)(py)2] (Pc = phthalocyaninato(2-)), as an effective catalyst in intramolecular C(sp3)-H bond amination, with alkyl azides as the nit
Synthesis of arylglycine and mandelic acid derivatives through carboxylations of α-amido and α-acetoxy stannanes with carbon dioxide
Mita, Tsuyoshi,Sugawara, Masumi,Hasegawa, Hiroyuki,Sato, Yoshihiro
experimental part, p. 2159 - 2168 (2012/06/01)
Incorporation reactions of carbon dioxide (CO2) with N-Boc-α-amido and α-acetoxy stannanes were developed using CsF as a mild tin activator. Monoprotected α-amido stannanes could be used, and the corresponding arylglycine derivatives were obtained in moderate-to-high yields under 1 MPa (10 atm) of CO2 pressure. α-Acetoxy stannanes also underwent carboxylation to afford mandelic acid derivatives in excellent yields under ambient CO2 pressure. Both transformations enabled the synthesis of α-tertiary and α-quaternary carboxylic acid derivatives. In addition, the chirality of (S)-N-tert-butylsulfonyl-α- amido stannanes was transferred with up to 90% inversion of configuration at 100 °C.
