32116-24-8 Usage
Description
2-Acetyl-4-nitro-1H-pyrrole is an organic compound with the molecular formula C6H6N2O3. It is a derivative of the pyrrole family, characterized by the presence of a nitrogen atom in the ring structure. 2-Acetyl-4-nitro-1H-pyrrole is known for its potential applications in the pharmaceutical and chemical industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
2-Acetyl-4-nitro-1H-pyrrole is used as a key intermediate in the synthesis of various pyrroles and indoles. These synthesized compounds have shown potential as antiviral agents, making 2-Acetyl-4-nitro-1H-pyrrole a valuable component in the development of new antiviral medications.
Used in Chemical Synthesis:
In the chemical industry, 2-Acetyl-4-nitro-1H-pyrrole serves as a versatile building block for the creation of a wide range of chemical compounds. Its unique structure allows for further functionalization and modification, leading to the development of new materials and products with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 32116-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,1 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32116-24:
(7*3)+(6*2)+(5*1)+(4*1)+(3*6)+(2*2)+(1*4)=68
68 % 10 = 8
So 32116-24-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O3/c1-4(9)6-2-5(3-7-6)8(10)11/h2-3,7H,1H3
32116-24-8Relevant articles and documents
Synthesis of 5-acetyl-2-aminopyrrole C-deoxyribonucleoside
Oda, Hiroshi,Hanami, Takeshi,Iwashita, Takashi,Kojima, Miki,Itoh, Masayoshi,Hayashizaki, Yoshihide
, p. 12747 - 12753 (2007)
A novel C-deoxyribonucleoside bearing 2-aminopyrrole was synthesized. The C-glycosidation between deoxyribose and pyrrole ring was carried out using palladium-catalyzed Heck coupling in the presence of excess amount of lithium chloride as an additive. The
Alkaloids from the traditional chinese medicine ChanSu: Synthesis-enabled structural reassignment of bufopyramide to bufoserotonin C
Davison, Emma K.,Sperry, Jonathan
supporting information, p. 7911 - 7914 (2015/07/27)
A synthesis of putative bufopyramide has shown the structure assigned to the natural product to be incorrect. The spectroscopic data for the natural product bufopyramide matches that obtained from a synthetic sample of bufoserotonin C, confirming that the
