111080-58-1 Usage
Chemical compound
A substance formed by the chemical combination of two or more elements in a fixed proportion.
Pyrrolidine derivative
A compound that is derived from pyrrolidine, a heterocyclic amine.
Benzyl group
A phenylmethyl group (C6H5CH2-) attached to a molecule.
Methyl group
A univalent alkyl group (-CH3) attached to a molecule.
Carboxamide functional group
A functional group with the structure -CONH2, consisting of a carbonyl group (C=O) bonded to an amine group (NH2).
Potential pharmacological and medicinal properties
The compound may have beneficial effects on human health and could be used in the development of drugs.
Neuroprotective agent
A substance that may protect neurons from damage or degeneration.
Treatment for neurodegenerative diseases
The compound may be used to treat conditions such as Alzheimer's and Parkinson's, which involve the progressive loss of nerve cells.
Analgesic
A substance that relieves pain without causing a loss of consciousness.
Anti-inflammatory agent
A substance that reduces inflammation in the body.
Ongoing research
Further studies are being conducted to better understand the properties and potential applications of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 111080-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,8 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111080-58:
(8*1)+(7*1)+(6*1)+(5*0)+(4*8)+(3*0)+(2*5)+(1*8)=71
71 % 10 = 1
So 111080-58-1 is a valid CAS Registry Number.
111080-58-1Relevant articles and documents
Α-substd. provitamin optically active production of phosphorus
-
Paragraph 0158; 0159, (2016/12/26)
PROBLEM TO BE SOLVED: To provide an industrial method practically suitable for producing an optically active α-substituted prolines with short process and mild conditions.SOLUTION: A method of producing an optically active α-substituted prolines (6) includes (d) a step of obtaining an optically active N, α-substituted prolines (5) by hydrolysis of an optically active N, α-substituted proline amides (4), and (e) a step of obtaining an optically active α-substituted prolines (6) by eliminating the optically active N, and a protective group Rof the α-substituted prolines (5).
Reactivity of a Cyclic α-Bromoiminium Bromide towards Nucleophiles
Donati, Donato,Fusi, Stefania,Macripo, Maria Adelaide,Ponticelli, Fabio
, p. 481 - 483 (2007/10/02)
Piperidine-pyrrolidine ring contraction of 1-piperideinium bromide (1) was observed by reaction with aqueous bases, sodium methoxide, phenylhydrazine, (S)-1-phenylethylamine and sodium borohydride, whereas diazomethane addition mainly gave pyrrolopyridine derivative 8.Some stereochemical features of these reactions have been investigated. 1 gave back bromine under suitable conditions.