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Atomfair (4-Methoxybenzyl)hydrazine C8H12N2O
Description (4-Methoxybenzyl)hydrazine (CAS No. 412327-07-2) is a high-purity organic compound with the molecular formula C8H12N2O . This specialized reagent, also known by its IUPAC name (4-methoxyphenyl)methylhydrazine , is widely utilized in pharmaceutical research, organic synthesis, and chemical intermediate applications. Its unique structure, featuring a methoxybenzyl group attached to a hydrazine moiety, makes it valuable for constructing complex heterocycles and active pharmaceutical ingredients (APIs). Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a crystalline solid or solution under inert packaging to maintain stability. Suitable for use in medicinal chemistry, asymmetric synthesis, and as a building…
Description
Description
(4-Methoxybenzyl)hydrazine (CAS No. 412327-07-2) is a high-purity organic compound with the molecular formula C8H12N2O. This specialized reagent, also known by its IUPAC name (4-methoxyphenyl)methylhydrazine, is widely utilized in pharmaceutical research, organic synthesis, and chemical intermediate applications. Its unique structure, featuring a methoxybenzyl group attached to a hydrazine moiety, makes it valuable for constructing complex heterocycles and active pharmaceutical ingredients (APIs). Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a crystalline solid or solution under inert packaging to maintain stability. Suitable for use in medicinal chemistry, asymmetric synthesis, and as a building block for biologically active compounds.
- CAS No: 412327-07-2
- Molecular Formula: C8H12N2O
- Molecular Weight: 152.19
- Exact Mass: 152.094963011
- Monoisotopic Mass: 152.094963011
- IUPAC Name: (4-methoxyphenyl)methylhydrazine
- SMILES: COC1=CC=C(C=C1)CNN
- Synonyms: (4-methoxybenzyl)hydrazine, 140-69-2, (4-methoxyphenyl)methylhydrazine, hydrazine, [(4-methoxyphenyl)methyl]-, [(4-methoxyphenyl)methyl]hydrazine
Application
(4-Methoxybenzyl)hydrazine serves as a key intermediate in the synthesis of pharmaceutical compounds, particularly those targeting CNS disorders. It is employed in the preparation of hydrazone derivatives for antimicrobial and anticancer research. The compound’s reactive hydrazine group facilitates Schiff base formation, making it valuable for catalyst development and polymer chemistry applications.
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