199328-27-3 Usage
Description
(4-cyano-2-nitro-phenyl)-acetic acid ethyl ester is a chemical compound with the molecular formula C11H10N2O4. It is an ethyl ester derivative of (4-cyano-2-nitro-phenyl)-acetic acid, which is a nitrophenylacetic acid derivative. This yellow crystalline solid is sparingly soluble in water but soluble in organic solvents such as ethanol and ether.
Uses
Used in Organic Synthesis:
(4-cyano-2-nitro-phenyl)-acetic acid ethyl ester is used as a building block in organic synthesis for the creation of various biologically active compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, (4-cyano-2-nitro-phenyl)-acetic acid ethyl ester serves as a key intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs.
Used in Antitumor Applications:
(4-cyano-2-nitro-phenyl)-acetic acid ethyl ester is utilized for its potential antitumor properties, playing a role in cancer treatment research.
Used in Anti-inflammatory Applications:
(4-cyano-2-nitro-phenyl)-acetic acid ethyl ester is also recognized for its potential anti-inflammatory properties, making it a candidate for use in treatments targeting inflammation.
Used as a Starting Material in Pharmaceutical Production:
(4-cyano-2-nitro-phenyl)-acetic acid ethyl ester is used as a starting material in the production of other compounds utilized within the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 199328-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,3,2 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 199328-27:
(8*1)+(7*9)+(6*9)+(5*3)+(4*2)+(3*8)+(2*2)+(1*7)=183
183 % 10 = 3
So 199328-27-3 is a valid CAS Registry Number.
199328-27-3Relevant articles and documents
A practical synthesis of 2-aryl-indole-6-carboxylic acids
Gallou, Fabrice,Yee, Nathan,Qiu, Fenghe,Senanayake, Chris,Linz, Guenter,Schnaubelt, Juergen,Soyka, Rainer
, p. 883 - 885 (2007/10/03)
A practical synthesis of 2-aryl-indole-6-carboxylic acids was developed via a sequence consisting of SNAr reaction, reductive cyclization, hydrolysis and decarboxylation. This process is efficient in terms of operational simplicity, cost effectiveness and is amenable to large scale production.
