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6-FLUOROQUINOLINE-2,3-DICARBOXYLIC ACID DIETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92525-75-2

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92525-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92525-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,5,2 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92525-75:
(7*9)+(6*2)+(5*5)+(4*2)+(3*5)+(2*7)+(1*5)=142
142 % 10 = 2
So 92525-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H14FNO4/c1-3-20-14(18)11-8-9-7-10(16)5-6-12(9)17-13(11)15(19)21-4-2/h5-8H,3-4H2,1-2H3

92525-75-2SDS

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 diethyl 6-fluoroquinoline-2,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names QU119

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:92525-75-2 SDS

92525-75-2Downstream Products

92525-75-2Relevant academic research and scientific papers

Selective reductive annulation reaction for direct synthesis of functionalized quinolines by a cobalt nanocatalyst

Xie, Rong,Lu, Guang-Peng,Jiang, Huan-Feng,Zhang, Min

, p. 239 - 243 (2020/02/15)

Due to the extensive applications of quinolines, the search for selective construction of such products has long been an attractive subject in scientific community. Herein, by developing a new N-doped ZrO2@C supported cobalt nanomaterial, it has been successfully applied as an efficient catalyst for the reductive annulation of 2-nitroaryl carbonyls with alkynoates and alkynones. The catalytic transformation allows synthesizing a wide array of funcitonalized quinolines with the merits of broad substrate scope, good functional group tolerance, excellent hydrogen transfer selectivity, reusable earth-abundant metal catalyst, and operational simplicity. The developed chemistry paves the ways for further design of hydrogen transfer-mediated coupling reactions by developing heterogeneous catalysts with suitable supports.

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