59557-91-4
59557-91-4
Chemical Structure
4-Bromo-2-methoxyaniline
- CAS. Nr.: 59557-91-4
- Formula:C7H8BrNO
- Molecular Weight:202.05
IUPAC Name: 4-bromo-2-methoxyaniline
InChIKey: WRFYIYOXJWKONR-UHFFFAOYSA-N
SMILES: NC1=CC=C(Br)C=C1OC
Biological Activity: 4-Bromo-2-methoxyaniline is a synthetic intermediate. 4-Bromo-2-methoxyaniline can be used in the synthesis of substituted anilines and brominated methoxyaniline derivatives[1][2][3].
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4-Bromo-2-methoxyaniline | 4-Bromo-2-methoxyaniline is a synthetic intermediate. 4-Bromo-2-methoxyaniline can be used in the synthesis of substituted anilines and brominated methoxyaniline derivatives. | |||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.88
HY-W3546932,4-Diaminoanisole -
Similarity Score 0.87
HY-W0078654-Bromo-2-methoxyphenol -
Similarity Score 0.87
HY-W0124165-Bromo-2-chloroanisole -
Similarity Score 0.85
HY-W0012132-Amino-4-methoxyphenol -
Similarity Score 0.84
HY-W0257365-Amino-2-methoxyphenol -
Similarity Score 0.84
HY-W0010942-Bromo-4-fluoroanisole -
Similarity Score 0.83
HY-W0158024-Methoxy-2-methylaniline -
Similarity Score 0.82
HY-W0076252-Amino-4-bromophenol -
Similarity Score 0.81
HY-Y01591-Bromo-2,4-dimethoxybenzene -
Explore the MedChemAI to find more analogs
References
- [1]. Takai T, et al. Design and synthesis of piperazine derivatives as a novel class of γ-secretase modulators that selectively lower Aβ₄₂ production. Bioorganic & medicinal chemistry. 2015 May 01;23(9):1923-34.
- [2]. Wang T, et al. Retrosynthesis of Wulfenioidins L with Potential Anti-Zika Virus Activity[C]//BIO Web of Conferences. EDP Sciences, 2024, 111: 02004.
- [3]. Malik Q M, et al. Synthesis and reactivity of dimethoxy-functionalised Tröger’s base analogues[J]. Tetrahedron, 2011, 67(32): 5798-5805.
