106380-95-4 Usage
Uses
Used in Pharmaceutical Industry:
3-Acetyl-2-methylquinoline-4-carboxylic acid, 97% is used as a building block for the synthesis of various pharmaceutical compounds. Its high purity and stability make it suitable for use in the development of new drugs and medications.
Used in Research Industry:
3-Acetyl-2-methylquinoline-4-carboxylic acid, 97% is used in organic synthesis and chemical research. Its unique chemical properties and structure make it a valuable tool for researchers studying the synthesis and properties of various compounds.
Used in Organic Synthesis:
3-Acetyl-2-methylquinoline-4-carboxylic acid, 97% is used as a key intermediate in the synthesis of complex organic compounds. Its reactivity and versatility allow for the creation of a wide range of chemical products.
Used in Chemical Research:
3-Acetyl-2-methylquinoline-4-carboxylic acid, 97% is used in chemical research to study its properties and potential applications. Its unique structure and reactivity make it an interesting subject for researchers exploring new chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 106380-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 106380-95:
(8*1)+(7*0)+(6*6)+(5*3)+(4*8)+(3*0)+(2*9)+(1*5)=114
114 % 10 = 4
So 106380-95-4 is a valid CAS Registry Number.
106380-95-4Relevant articles and documents
An improved Pfitzinger reaction: Eco-efficient synthesis of quinaldine-4-carboxylates by TMSCl-mediated
Lu, Lingling,Zhou, Pan,Hu, Biao,Li, Xiang,Huang, Rong,Yu, Fuchao
supporting information, p. 3658 - 3661 (2017/08/23)
We report herein an improved Pfitzinger reaction for the synthesis of highly functionalized quinaldines from 1,3-dicarbonyl compounds, isatins and alcohols mediated by TMSCl. This synthesis involves cyclization and esterification in one-step cascade process for the formation of a carboxylate (CO2R) at the 4-position of quinaldine ring. Moreover, this procedure shows highly efficient, good functional group tolerance, operational simplicity, environment-friendly and feasibility of scale up.
A simple one-pot synthesis of quinoline-4-carboxylic acid derivatives by Pfitzinger reaction of isatin with ketones in water
Lv, Qinghua,Fang, Lizhen,Wang, Pengfei,Lu, Chenjuan,Yan, Fulin
, p. 391 - 394 (2013/05/21)
An improved Pfitzinger condensation reaction performed under acidic conditions is established. It provides a simple and efficient synthetic method for some useful quinoline-4-carboxylic acid derivatives using isatins and ketones that cannot be obtained ea
