14000-66-9 Usage
Uses
Used in Pharmaceutical Synthesis:
4-(2-Hydroxyethyl)-piperazin-1-carboxylic acid ethyl ester is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex organic compounds, enhancing the development of new medications.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 4-(2-Hydroxyethyl)-piperazin-1-carboxylic acid ethyl ester is used as a building block for the creation of various organic compounds, leveraging its reactivity and solubility properties to facilitate chemical reactions.
Used in Research and Development:
4-(2-Hydroxyethyl)-piperazin-1-carboxylic acid ethyl ester is employed in research and development work within the pharmaceutical industry, where its unique properties may contribute to the discovery and innovation of novel therapeutic agents and chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 14000-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,0 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14000-66:
(7*1)+(6*4)+(5*0)+(4*0)+(3*0)+(2*6)+(1*6)=49
49 % 10 = 9
So 14000-66-9 is a valid CAS Registry Number.
14000-66-9Relevant academic research and scientific papers
Studies on hypotensive agents. Synthesis of 1-substituted 3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-2,4(1H,3H)- quinazolinediones
Eguchi,Sasaki,Sugimoto,Ebisawa,Ishikawa
, p. 1753 - 1759 (2007/10/02)
3-(2-Chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-2,4(1H,3H)- quinazolinedione was newly prepared. 1-Hydrogen atoms of the compound were variously substituted in order to test for their hypotensive activities on relaxing effects of the blood vessels. The compounds with 2-(1-pyrrolidinyl ethyl, 2-(1-piperidinyl)ethyl, 3-(dimethylamino)propyl, and 3-(N-benzyl-N-methylamino)propyl moieties showed significant activity. The 2-(1-piperidinyl)ethyl compound possessed activity approximately 23 times more potent than papaverine, however, it was less potent than cinnarizine.
