CAS 1145-76-2: Benzyl 4-nitrophenyl ether
Formula:C13H11NO3
InChI:InChI=1S/C13H11NO3/c15-14(16)12-6-8-13(9-7-12)17-10-11-4-2-1-3-5-11/h1-9H,10H2
InChI key:InChIKey=YOVUXLHIVNBVKO-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=CC=C(N(=O)=O)C=C2
Synonyms:- 1-(Benzyloxy)-4-Nitrobenzene
- 1-Nitro-4-(phenylmethoxy)benzene
- 1-Nitro-4-phenylmethoxybenzene
- 4-(Benzyloxy)nitrobenzene
- Benzene, 1-nitro-4-(phenylmethoxy)-
- Benzyl 4-nitrophenyl ether
- Benzyl p-nitrophenyl ether
- Ether, benzyl p-nitrophenyl
- NSC 24667
- [(4-Nitrophenoxy)methyl]benzene
- p-(Benzyloxy)nitrobenzene
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Found 6 products.
Benzene, 1-nitro-4-(phenylmethoxy)-
CAS:Formula:C13H11NO3Purity:95%Color and Shape:SolidMolecular weight:229.23131-Benzyloxy-4-nitrobenzene
CAS:Formula:C13H11NO3Purity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:229.241-(Benzyloxy)-4-nitrobenzene
CAS:Purity:98.0%Color and Shape:SolidMolecular weight:229.235000610351561-(Benzyloxy)-4-nitrobenzene
CAS:1-(Benzyloxy)-4-nitrobenzene is a chemical that is used in organic synthesis. It reacts with sodium hydrogen sulfate to form anilines, which are useful for the production of dyes and pharmaceuticals. The reaction mechanism involves the formation of a benzyloxy nitroso intermediate, followed by the addition of hydrogen sulfate. The reaction rate depends on the hydration of 1-(benzyloxy) 4-nitrobenzene and the presence of a functional group. The conjugates formed during this reaction are stable, which aids in its reactivity.Formula:C13H11NO3Purity:Min. 95%Molecular weight:229.23 g/molRef: 3D-FB131130
Discontinued product
