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17133-54-9

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17133-54-9 Usage

General Description

(3,4-Dihydro-2H-quinolin-1-yl)-acetic acid Methyl ester is a chemical compound that belongs to the class of quinoline derivatives. It is a methyl ester of (3,4-Dihydro-2H-quinolin-1-yl)-acetic acid, which is a synthetic intermediate used in the production of pharmaceuticals and agrochemicals. (3,4-Dihydro-2H-quinolin-1-yl)-acetic acid Methyl ester has potential pharmacological activities and is under study for its potential use as a drug candidate. It has a quinoline backbone, which is known for its diverse biological activities and is being investigated for its therapeutic potential in various diseases. Overall, (3,4-Dihydro-2H-quinolin-1-yl)-acetic acid Methyl ester is a chemical with potential pharmaceutical applications and is the subject of ongoing research and development.

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.

17133-54-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(3,4-dihydro-2H-quinolin-1-yl)acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17133-54-9 SDS

17133-54-9Downstream Products

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.

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