67514-33-4 Usage
Chemical Class
Piperazine derivatives
Molecular Structure
Contains a piperazine ring
Includes an allyl group
Consists of a propanol chain
Functional Groups
Piperazine ring: Provides potential pharmacological activity and versatility in drug synthesis.
Allyl group: Imparts reactivity and flexibility for further chemical modifications.
Propanol chain: Determines solubility and compatibility with various solvents and reaction conditions.
Potential Applications
Pharmaceutical Intermediate: Used in the synthesis of diverse drugs due to its structural features and reactivity.
Chemical Building Block: Serves as a precursor for the synthesis of other organic compounds, enhancing molecular complexity.
Biological Activity
Neurotransmitter Modulator: The presence of piperazine and alcohol functional groups suggests potential activity in modulating neurotransmitter systems.
Versatility
Pharmaceutical Industry: Offers opportunities for drug development and synthesis.
Chemical Industry: Utilized in the production of various organic compounds.
Research: Investigated for potential pharmacological and biochemical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 67514-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,1 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67514-33:
(7*6)+(6*7)+(5*5)+(4*1)+(3*4)+(2*3)+(1*3)=134
134 % 10 = 4
So 67514-33-4 is a valid CAS Registry Number.
67514-33-4Relevant articles and documents
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.
