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ethyl 4-chloro-6,7,8-trifluoroquinoline-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

207231-24-1

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207231-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207231-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,2,3 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 207231-24:
(8*2)+(7*0)+(6*7)+(5*2)+(4*3)+(3*1)+(2*2)+(1*4)=91
91 % 10 = 1
So 207231-24-1 is a valid CAS Registry Number.

207231-24-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-chloro-6,7,8-trifluoroquinoline-3-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 6,7,8-trifluoro-4-chloro-quinoline-3-carboxylate

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:207231-24-1 SDS

207231-24-1Downstream Products

207231-24-1Relevant articles and documents

Development of a practical and efficient synthesis of SIPI-4884, a HMG CoA reductase inhibitor for the treatment of hypercholesterolemia

Hao, Qun,Pan, Jing,Li, Yongjia,Cai, Zhengyan,Zhou, Weicheng

, p. 921 - 926 (2013/07/26)

An improved process of the novel HMG CoA reductase inhibitor SIPI-4884 has been developed for early preclinical pharmacology and safety studies, and it was made up with an efficient nine-step and scalable process. Significant improvements in the nucleophi

Quinoline Compounds, Intermediates, Preparation Methods and Uses Thereof

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Page/Page column 5, (2011/04/14)

A kind of quinoline compounds as formula A, pharmaceutical accepted solvates, optical isomers or polymorphisms thereof. The intermediates of formula D. in which, R1, R2 and R3 is independently H, halo or the subustitents o

THERAPEUTIC PYRAZOLOQUINOLINE DERIVATIVES

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Page/Page column 51, (2009/01/20)

The invention provides a novel chemical series of formula I, as well as methods of use thereof for binding to the benzodiazepine site of the GABAA receptor and modulating GABAA, and use of the compound of formula I for the treatment of GABAA receptor associated disorders. The general structure of formula I is shown below and can exist in tautomeric forms: The invention further provides a method of modulation of one or more GABAA subtypes in an animal comprising administering to the animal an effective amount of a compound of formula (I).

High affinity central benzodiazepine receptor ligands: Synthesis and structure-activity relationship studies of a new series of pyrazolo[4,3- c]quinolin-3-ones

Savini,Massarelli,Nencini,Pellerano,Biggio,Maciocco,Tuligi,Carrieri,Cinone,Carotti

, p. 389 - 399 (2007/10/03)

A large series of 2-aryl(heteroaryl)-2,5-dihydropyrazolo[4,3-c]quinolin- 3-(3H)-ones, carrying appropriate substituents at the quinoline and N2- phenyl rings, were prepared and tested as central benzodiazepine receptor ligands. Results from structure-affinity relationship studies were in full agreement with previously proposed pharmacophore models and, in addition, quantitative structure-activity analysis gave further significant insight into the main molecular determinants of high benzodiazepine receptor affinity. The intrinsic activity of some active ligands was also determined and preliminary discussed.

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