1074-54-0 Usage
Uses
Used in Pharmaceutical Industry:
Alpha-methylpiperazine-1-ethanol is used as a precursor in the synthesis of pharmaceutical drugs for its ability to contribute to the formation of various medicinal compounds, enhancing the development of new therapeutic agents.
Used in Chemical Industry:
alpha-methylpiperazine-1-ethanol is utilized as a solvent due to its ability to dissolve a wide range of substances, facilitating various chemical reactions and processes.
Used in Corrosion Inhibition:
Alpha-methylpiperazine-1-ethanol is used as a corrosion inhibitor to protect metal surfaces from degradation, extending the lifespan of materials used in various industrial applications.
Used in Pesticide Production:
It serves as an intermediate in the manufacture of pesticides, contributing to the development of effective agricultural chemicals to protect crops.
Used in Surfactant Synthesis:
Alpha-methylpiperazine-1-ethanol is used in the production of surfactants, which are essential in creating stable dispersions and emulsions in various consumer and industrial products.
Used in Polymer Production:
alpha-methylpiperazine-1-ethanol is employed in the synthesis of polymers, which are used in a wide array of applications, from plastics to textiles, due to its ability to influence polymer properties.
Used in Photography and Color Film Processing:
Alpha-methylpiperazine-1-ethanol is used as a stabilizer in photography and color film processing to ensure the longevity and quality of the final product.
Used in Therapeutic Applications:
It has been investigated for its potential use as a therapeutic agent in the treatment of certain medical conditions, highlighting its possible impact on healthcare and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 1074-54-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1074-54:
(6*1)+(5*0)+(4*7)+(3*4)+(2*5)+(1*4)=60
60 % 10 = 0
So 1074-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O/c1-7(10)6-9-4-2-8-3-5-9/h7-8,10H,2-6H2,1H3
1074-54-0Relevant academic research and scientific papers
Producing polyurethanes using hydroxy-alkyl piperazine catalyst compositions
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, (2008/06/13)
Disclosed is a catalytic composition comprising a substance having the general formula: STR1 where R1 is an alkyl group having 1 to 3 C atoms and R2 is a group selected from --H, --CH3 and CH2 CH3. The catalytic composition is odorless and excellent in the urethane forming reaction in production of polyurethane.
SYNTHESES OF PIPERAZINES SUBSTITUTED ON THE NITROGEN ATOMS WITH ALLYL, PROPYL, 2-HYDROXYPROPYL AND 3-HYDROXYPROPYL GROUPS
Kafka, Stanislav,Cermak, Jan,Novak, Tomas,Pudil, Frantisek,Viden, Ivan,Ferles, Miloslav
, p. 1201 - 1211 (2007/10/02)
The paper describes synthesis of 1,4-diallylpiperazine (I), 1-allylpiperazine (III), 1-propylpiperazine (IV), 1-(1-piperazinyl)-2-propanol (V), 3-(1-piperazinyl)-1-propanol (VI), 1-allyl-4-propylpiperazine (VII), 1-(4-allyl-1-piperazinyl)-2-propanol (VIII), 3-(4-allyl-1-piperazinyl)-1-propanol (IX), 1,4-dipropylpiperazine (X), 1-(4-propyl-1-piperazinyl)-2-propanol (XI), 3-(4-propyl-1-piperazinyl)-1-propanol (XII), 1,4-bis(2-hydroxypropyl)piperazine (XIII), 3--1-propanol (XIV) and 1,4-bis(3-hydroxypropyl)piperazine (XV).Retention indices of I-XV are reported and mass spectra of the compounds are discussed.
HYDROBORATION OF 1,4-DIALLYLPIPERAZINE
Kafka, Stanislav,Ferles, Miloslav
, p. 2275 - 2283 (2007/10/02)
Hydroboration of 1,4-diallylpiperazine (I) with triethylamine-borane afforded 5,8-diaza-1,9-diboradispirotetradecane (II). 1,4-Diallylpiperazine dihydrochloride reacted with sodium borohydride to give 1,4-diallylpiperazine-diborane (V).Ethanolysis of II furnished 1,4-bis(3-diethoxyborylpropyl)piperazine (IV).The products of hydroboration of I were subjected to hydrolysis with hydrochloric acid and subsequent oxidation with alkaline hydrogen peroxide and the obtained mixtures were analyzed by gas-liquid chromatography and mass spectrometry.
