17133-54-9 Usage
Description
(3,4-Dihydro-2H-quinolin-1-yl)-acetic acid Methyl ester is a quinoline derivative that serves as a synthetic intermediate in the production of pharmaceuticals and agrochemicals. It possesses a quinoline backbone, which is known for its diverse biological activities and is being investigated for its therapeutic potential in various diseases.
Uses
Used in Pharmaceutical Industry:
(3,4-Dihydro-2H-quinolin-1-yl)-acetic acid Methyl ester is used as a synthetic intermediate for the development of pharmaceuticals. Its potential pharmacological activities make it a promising candidate for drug discovery and therapeutic applications in various diseases.
Used in Agrochemical Industry:
(3,4-Dihydro-2H-quinolin-1-yl)-acetic acid Methyl ester is also used as a synthetic intermediate in the production of agrochemicals. Its potential applications in this industry may include the development of pesticides, herbicides, or other agricultural chemicals to improve crop yield and protect against pests.
Overall, (3,4-Dihydro-2H-quinolin-1-yl)-acetic acid Methyl ester is a chemical compound with potential applications in both the pharmaceutical and agrochemical industries, and its ongoing research and development aim to unlock its full potential in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 17133-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,3 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17133-54:
(7*1)+(6*7)+(5*1)+(4*3)+(3*3)+(2*5)+(1*4)=89
89 % 10 = 9
So 17133-54-9 is a valid CAS Registry Number.
17133-54-9Relevant articles and documents
Inactivation of myostatin by photo-oxygenation using catalyst-functionalized peptides
Okamoto, Hideyuki,Taniguchi, Atsuhiko,Usami, Shoya,Taguchi, Akihiro,Takayama, Kentaro,Hayashi, Yoshio
supporting information, p. 9108 - 9111 (2019/08/07)
Inhibition of myostatin is an attractive treatment for muscular dystrophy and other amyotrophic diseases. A myostatin-binding peptide was functionalized by equipped with an on/off switchable photo-oxygenation catalyst. This peptide induces a selective oxygenation of myostatin under near-infrared light, resulting in inactivation of myostatin. This peptide shows several orders of magnitude greater inhibitory effect than the original peptide.
Transition-metal-free decarboxylation of dimethyl malonate: An efficient construction of α-amino acid esters using TBAI/TBHP
Zhang, Jie,Shao, Ying,Wang, Yaxiong,Li, Huihuang,Xu, Dongmei,Wan, Xiaobing
, p. 3982 - 3987 (2015/03/30)
A transition-metal-free decarboxylation coupling process for the preparation of α-amino acid esters, which succeeded in merging hydrolysis/decarboxylation/nucleophilic substitution, is well described. This strategy uses commercially available inexpensive starting materials, catalysts and oxidants and has a wide substrate scope and operational simplicity. This journal is
Pharmaceutical compounds
-
, (2008/06/13)
This invention relates to compounds of formula (I) where R1 to R12, —W—V—, —X—Y—, m and n have the values defined in claim 1, their preparation and use as pharmaceuticals.
