93454-25-2 Usage
Molecular weight
415.45 g/mol
Structure
The compound consists of a pyrroloindole core structure, with a phenylmethyl ester group and an acetylamino group attached to the molecule.
Functional groups
The compound contains an ester group (phenylmethyl ester), an acetylamino group, a ketone group, and a carboxylic acid group.
Stereochemistry
The compound is hexahydro, indicating that it contains six hydrogen atoms in a cyclic structure.
Substitution patterns
The compound has a methyl group at the 6-position and a phenylmethyl ester group at the 8-position.
Biological activity
The compound has potential applications in medicinal chemistry and drug development due to its structural versatility and potential biological activities.
Solubility
The compound's solubility properties are not specified, but it is likely to be soluble in organic solvents such as DMSO or methanol.
Stability
The compound's stability properties are not specified, but it is likely to be stable under standard laboratory conditions.
Synthesis
The synthesis of 1H-Pyrrolo[1,2-a]indole-9-carboxylic acid,
2-(acetylamino)-2,3,5,6,7,8-hexahydro-6-methyl-8-oxo-, phenylmethyl
ester would involve multiple steps, including the formation of the pyrroloindole core structure, the attachment of the functional groups, and the formation of the ester bond.
Check Digit Verification of cas no
The CAS Registry Mumber 93454-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,5 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93454-25:
(7*9)+(6*3)+(5*4)+(4*5)+(3*4)+(2*2)+(1*5)=142
142 % 10 = 2
So 93454-25-2 is a valid CAS Registry Number.
93454-25-2Relevant academic research and scientific papers
Total Synthesis of a Mitosene
Rebek, Julius,Shaber, Steven H.,Shue, Youe-Kong,Gehret, Jean-Claude,Zimmerman, Stephen
, p. 5164 - 5174 (2007/10/02)
The total synthesis of a mitosene (a chemical degradation product of mitomycin C) is described.The synthesis begins with hydroxyproline and uses a Huisgen pyrrole synthesis to form a pyrrolizidine system.The carbocyclic ring is made through Dieckmann cycl
