35229-84-6 Usage
General Description
ETHYL 2-CHLORO-2-(2-[3-(TRIFLUOROMETHYL)PHENYL]-HYDRAZONO)ACETATE is a chemical compound that consists of an ethyl ester group attached to a chloro-substituted acetate group, which is in turn connected to a hydrazono group linked to a trifluoromethyl phenyl ring. It is commonly used as a reagent in organic synthesis and pharmaceutical research due to its potential as a building block for more complex organic molecules. ETHYL 2-CHLORO-2-(2-[3-(TRIFLUOROMETHYL)PHENYL]-HYDRAZONO)ACETATE may also have applications in the development of new drugs or materials due to its unique structure and potential reactivity. It is important to handle and use this chemical with care, following all proper safety protocols and guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 35229-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35229-84:
(7*3)+(6*5)+(5*2)+(4*2)+(3*9)+(2*8)+(1*4)=116
116 % 10 = 6
So 35229-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H10ClF3N2O2/c1-2-19-10(18)9(12)17-16-8-5-3-4-7(6-8)11(13,14)15/h3-6,16H,2H2,1H3/b17-9+
35229-84-6Relevant articles and documents
A new method for the synthesis of 1-aryl-1,2,4-triazole derivatives
Matiychuk, Vasyl S.,Potopnyk, Mykhaylo A.,Luboradzki, Roman,Obushak, Mykola D.
experimental part, p. 1799 - 1803 (2011/07/08)
A new and convenient one-step recyclization method for the synthesis of ethyl 1-aryl-5-oxo-4,5-dihydro-1H-1,2,4-triazole-3-carboxylates is reported. Various ethyl chloro(2-arylhydrazinylidene)ethanoates react with thiazolidine-2,4-dione in the presence of potassium hydroxide to produce the 1-aryl-1,2,4-triazole derivatives in moderate to good yields. The procedure is economical, environmentally friendly and simple to perform. Georg Thieme Verlag Stuttgart - New York.
Phytotoxic activity in pyrazole derivatives. I
Bernard,Cocco,Maccioni,Plumitallo
, p. 259 - 271 (2007/10/02)
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