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Ethyl 4-chloro-6,7-difluoroquinoline-3-carboxylate is a complex chemical compound derived from the quinoline family, featuring a quinoline ring with multiple functional groups. It is characterized by the presence of an ethyl ester group at the 3-carboxylate position, and chlorine and difluoro substituents at the 4 and 6,7 positions, respectively. Ethyl 4-chloro-6,7-difluoroquinoline-3-carboxylate is widely recognized for its utility in organic synthesis and pharmaceutical research, where it serves as a key intermediate in the development of innovative drugs and biologically active molecules.

318685-01-7

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  • SAGECHEM/Ethyl 4-chloro-6,7-difluoroquinoline-3-carboxylate/SAGECHEM/Manufacturer in China

    Cas No: 318685-01-7

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318685-01-7 Usage

Uses

Used in Pharmaceutical Research and Development:
Ethyl 4-chloro-6,7-difluoroquinoline-3-carboxylate is utilized as a crucial intermediate in the synthesis of new pharmaceuticals, particularly for the creation of drugs targeting various diseases and conditions. Its unique structure and reactivity allow for the development of molecules with enhanced properties and therapeutic effects.
Used in Organic Synthesis:
In the field of organic synthesis, Ethyl 4-chloro-6,7-difluoroquinoline-3-carboxylate is employed as a versatile building block for the construction of complex organic molecules. Its functional groups enable a range of chemical reactions, facilitating the synthesis of diverse compounds with potential applications in various industries.
Used in Agrochemical Production:
Ethyl 4-chloro-6,7-difluoroquinoline-3-carboxylate also finds application in the agrochemical industry, where it is used as a precursor for the synthesis of bioactive molecules with pesticidal properties. Its incorporation into agrochemicals can contribute to the development of more effective and targeted pest control solutions.
Used in Chemical Modification for Enhanced Derivatives:
The unique structure of Ethyl 4-chloro-6,7-difluoroquinoline-3-carboxylate makes it an attractive target for chemical modification. Researchers can manipulate its functional groups to create new derivatives with potentially improved properties, broadening its scope of applications in various fields, including medicine, agriculture, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 318685-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,8,6,8 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 318685-01:
(8*3)+(7*1)+(6*8)+(5*6)+(4*8)+(3*5)+(2*0)+(1*1)=157
157 % 10 = 7
So 318685-01-7 is a valid CAS Registry Number.

318685-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-chloro-6,7-difluoroquinoline-3-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 4-chloro-6,7-difluoro-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:318685-01-7 SDS

318685-01-7Downstream Products

318685-01-7Relevant articles and documents

Cyclopropanation–ring expansion of 3-chloroindoles with α-halodiazoacetates: Novel synthesis of 4-quinolone-3-carboxylic acid and norfloxacin

Peeters, Sara,Berntsen, Linn Neerbye,Rongved, P?l,Bonge-Hansen, Tore

supporting information, p. 2156 - 2160 (2019/09/30)

We present a short and efficient way of synthesizing two synthetically versatile 4-quinolone-3-carboxylate building blocks by cyclopropanation-ring expansion of 3-chloroindoles with α-halodiazoacetates as the key step. This novel transformation was applied towards the synthesis of the antibiotic drug norfloxacin.

THERAPEUTIC PYRAZOLOQUINOLINE UREA DERIVATIVES

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Page/Page column 19, (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

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