100-19-6
100-19-6
Chemical Structure
4'-Nitroacetophenone
- CAS No.: 100-19-6
- Formula:C8H7NO3
- Molecular Weight:165.15
IUPAC Name: 1-(4-nitrophenyl)ethanone
InChIKey: YQYGPGKTNQNXMH-UHFFFAOYSA-N
SMILES: CC(C1=CC=C([N+]([O-])=O)C=C1)=O
Biological Activity: 4'-Nitroacetophenone is a nitroaromatic compound. 4'-Nitroacetophenone is an important organic synthetic intermediate, which can be used for the synthesis of other active compounds such as Chloramphenicol (HY-B0239)[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4'-Nitroacetophenone | 99.69% | 4'-Nitroacetophenone is a nitroaromatic compound. 4'-Nitroacetophenone is an important organic synthetic intermediate, which can be used for the synthesis of other active compounds such as Chloramphenicol (HY-B0239). | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.93
HY-321441-(3-Nitrophenyl)ethanone -
Similarity Score 0.88
HY-Y0607R4-Nitrobenzoic acid (Standard) -
Similarity Score 0.85
HY-41464Ethyl 4-nitrobenzoate -
Similarity Score 0.83
HY-W007577R4-Nitrobenzaldehyde (Standard) -
Similarity Score 0.83
HY-Y13133-Nitrobenzoic acid -
Similarity Score 0.83
HY-34158N-(4-Nitrophenethyl)acetamide -
Similarity Score 0.81
HY-30374Tamsulosin impurity 4 -
Similarity Score 0.80
HY-W0150694-Nitrocinnamic acid -
Similarity Score 0.80
HY-W0155704-Nitrobenzyl alcohol -
Explore the MedChemAI to find more analogs
References
- [1]. KLOSA J. et al [Studies on the exchange of diazonium group with nitro group for the preparation of p-nitroacetophenone. III. Synthesis of chloramphenicol]. Arch Pharm Ber Dtsch Pharm Ges. 1953;286(8):416-8. Undetermined Language. [Content Brief]
- [2]. Pérez-Rebolledo A, et al. 4-nitroacetophenone-derived thiosemicarbazones and their copper(II) complexes with significant in vitro anti-trypanosomal activity. Eur J Med Chem. 2008 May;43(5):939-48. [Content Brief]
- [3]. Alam A, et al. Novel Bis-Schiff's base derivatives of 4-nitroacetophenone as potent α-glucosidase agents: Design, synthesis and in silico approach. Bioorg Chem. 2022 Nov;128:106058. [Content Brief]
