111573-52-5 Usage
Main properties
1. Molecular formula: C5H5N3O
2. Heterocyclic compound
3. Cyclic imide derivative
4. Also known as imidazo[1,2-c]pyrrolo[1,2-a]pyridine-7,9-dione
5. Potential applications in medicinal chemistry
6. Interesting biological activities
7. Important building block for synthesis of various organic compounds
8. Potential uses in material science
Specific content
1. Molecular formula: C5H5N3O
2. Heterocyclic compound: Contains a ring structure with at least two different elements, in this case nitrogen and oxygen atoms.
3. Cyclic imide derivative: Contains an imide functional group, which is a specific type of organic compound containing a nitrogen atom bound to a carbon atom in a carbonyl group.
4. Potential applications in medicinal chemistry: Can be used in the development of pharmaceutical drugs due to its unique biological activities.
5. Interesting biological activities: Possesses properties that make it a promising target for drug discovery and development, indicating potential therapeutic benefits.
6. Important building block for synthesis of various organic compounds: Can be used as a key component in the creation of complex organic molecules in the pharmaceutical and agrochemical industries.
7. Potential uses in material science: Can be utilized in developing new materials and functional molecules, suggesting potential advancements in material technology.
Check Digit Verification of cas no
The CAS Registry Mumber 111573-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,7 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111573-52:
(8*1)+(7*1)+(6*1)+(5*5)+(4*7)+(3*3)+(2*5)+(1*2)=95
95 % 10 = 5
So 111573-52-5 is a valid CAS Registry Number.
111573-52-5Relevant articles and documents
A stereospecific route to (Z)-Urocanic acids
Despinoy, Xavier L. M.,McNab, Hamish,Tyas, Richard G.
, p. 1676 - 1678 (2008/12/22)
(Z)-Urocanic acid and its derivatives can be made stereo-specifically by ring-opening of pyrrolo[l,2-c]imidazol-5-ones in aqueous tetrahydrofuran.
New synthetic routes to pyrrolo-[1,2-a]- and -[1,2-c]-imidazol-5-ones by flash vacuum pyrolysis
McNab, Hamish,Thornley, Craig
, p. 2203 - 2209 (2007/10/03)
1-Substituted and 1,3-disubstituted pyrrolo[1,2-c]imidazol-5-ones 25-27 have been made in fair to excellent yield by flash vacuum pyrolysis (FVP) of the Meldrum's acid precursors 11-13. FVP of the appropriate propenoate precursor 23, 22 and 18-20 gives pyrrolo[1,2-c]imidazol-5-one 2, pyrrolo[1,2-a]-imidazol-5-one 3 and their 6-methyl derivatives 28-30 respectively in 32-90% yield. The mechanism of the propenoate pyrolyses involves rate determining E to Z isomerisation of the alkene followed by elimination of an alcohol and electrocyclisation to the fused ring products.
