85803-50-5 Usage
Uses
Used in Scientific Research:
3-Thiophen-2-yl-piperazine-1-carboxylic acid ethyl ester is used as a research chemical for [application reason] in the field of organic chemistry. Its unique molecular structure and moderate polarity make it a valuable compound for exploring various chemical reactions and interactions.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 3-Thiophen-2-yl-piperazine-1-carboxylic acid ethyl ester is used as a potentially active pharmaceutical intermediate. Its complex synthesis and precise conditions required for its production make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Organic Chemistry:
3-Thiophen-2-yl-piperazine-1-carboxylic acid ethyl ester is used as a key component in organic chemistry for [application reason]. Its central piperazine ring and attached functional groups provide a versatile platform for the synthesis of various organic compounds and the study of their properties and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 85803-50-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,0 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85803-50:
(7*8)+(6*5)+(5*8)+(4*0)+(3*3)+(2*5)+(1*0)=145
145 % 10 = 5
So 85803-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O2S/c1-2-15-11(14)13-6-5-12-9(8-13)10-4-3-7-16-10/h3-4,7,9,12H,2,5-6,8H2,1H3
85803-50-5Relevant academic research and scientific papers
Tetracyclic heterocycles and antidepressant compositions thereof
-
, (2008/06/13)
Tetracyclic heterocycles of the formula STR1 wherein Th is the residue completing a fused thiophen ring, X represents oxo, hydroxyl together with hydrogen, or preferably two hydrogens, R1 represents lower alkyl, lower alkoxy, chloro, bromo, trifluoromethyl or, preferably, hydrogen, and R2 represents hydroxy-lower alkyl, aryl-lower alkyl, or, preferably, lower alkyl, especially methyl, or hydrogen, and therapeutically acceptable acid addition salts thereof are especially useful as antidepressants, in particular in the form of appropriate pharmaceutical compositions. They are obtainable by conventional synthetic methods of organic chemistry.
Synthesis and biological properties of thiophene ring analogues of mianserin.
Watthey,Gavin,Desai,Finn,Rodebaugh,Patt
, p. 1116 - 1122 (2007/10/02)
The synthesis of two thiophene-containing analogues of mianserin, i.e., 1,2,3,4,10,13b-hexahydro-2-methylpiperazino[1,2-a]thieno[2, 3-c][1]benzazepine (2), and the corresponding [3,2-c] isomer (12) is described. The key step in the synthesis is the nucleo
