62407-64-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This is the IUPAC name of the compound, which provides a systematic way to name organic compounds based on their structure.
Explanation
A common name is a simpler, more easily recognizable name for a compound, often used in everyday language.
Explanation
Organic compounds are chemical compounds containing carbon and hydrogen atoms, often with other elements such as oxygen and nitrogen.
Explanation
The structure of the compound is described by the arrangement of its atoms and the types of chemical bonds between them.
Explanation
Alaptide is used primarily as a medicinal drug, indicating its potential therapeutic benefits.
Explanation
Alaptide has been studied for its potential to protect neurons and improve outcomes in various neurological conditions.
Explanation
The compound's pharmacological properties, which include its interactions with biological targets and its effects on the body, are still being researched.
Explanation
Alaptide's potential medical applications are being explored, particularly in the treatment of neurological conditions such as stroke, brain injury, and neurodegenerative diseases.
Type
Organic compound
Structure
Contains a triazolidine-3,5-dione ring, a 1-acetyl-2-methyl-2-propenyl group, and a phenyl group
Application
Medicinal drug
Neuroprotective agent
Potential therapeutic benefits for conditions such as ischemic stroke, traumatic brain injury, and neurodegenerative diseases
Pharmacological properties
Under investigation
Medical applications
Potential for use in treating neurological conditions
Check Digit Verification of cas no
The CAS Registry Mumber 62407-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,0 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62407-64:
(7*6)+(6*2)+(5*4)+(4*0)+(3*7)+(2*6)+(1*4)=111
111 % 10 = 1
So 62407-64-1 is a valid CAS Registry Number.
62407-64-1Relevant academic research and scientific papers
Ene-type adducts from the reaction of 4-phenyl-1,2,4-triazoline-3,5-dione with β-alkyl s-cis enones
Hunter, Norman Robert,Krawchuk, Bert Paul,Shiloff, Janice Deborah
, p. 835 - 839 (2007/10/02)
The adducts from the reaction of 4-phenyl-1,2,4-triazoline-3,5-dione with a number of α,β-unsaturated ketones have been isolated and characterized.The reaction generally proceeds with migration of the double bond to the β,γ-position and is highly chemoselective towards reaction with enones which have , or can assume, an s-cis conformation.
Regio- and Stereoselectivity in the Ene Reaction of N-Phenyl-1,2,4-triazoline-3,5-dione with α,β-Unsaturated Carbonyl Substrates
Hoye, Thomas R.,Bottorff, Kyle J.,Caruso, Andrew J.,Dellaria, Joseph F.
, p. 4287 - 4292 (2007/10/02)
N-Phenyltriazoline-3,5-dione reacts with α,β-unsaturated ketones,esters, and lactones 1a-l to give ene adducts 2a-l.The reactions usually proceed in good yield with high regioselectivity and, where possible, high stereoselectivity.Ene substrates capable of adopting an s-cis conformation show much greater reactivity.A variety of mechanistic interpretations is considered.
