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Atomfair (4-Methoxybenzyl)hydrazine dihydrochloride C8H14Cl2N2O CAS 412327-07-2
(4-Methoxybenzyl)hydrazine dihydrochloride (CAS No. 412327-07-2) is a high-purity organic compound with the molecular formula C8H14Cl2N2O . This white to off-white crystalline powder is a valuable hydrazine derivative extensively used in pharmaceutical research, organic synthesis, and chemical intermediates. With a purity of ≥95%, it serves as a key reagent in the preparation of heterocyclic compounds, Schiff bases, and other bioactive molecules. The dihydrochloride salt form enhances stability and solubility in aqueous solutions, making it suitable for controlled reactions. Store in a cool, dry place away from light and moisture to maintain integrity. Ideal for researchers and scientists requiring precise and reliable…
Description
(4-Methoxybenzyl)hydrazine dihydrochloride (CAS No. 412327-07-2) is a high-purity organic compound with the molecular formula C8H14Cl2N2O. This white to off-white crystalline powder is a valuable hydrazine derivative extensively used in pharmaceutical research, organic synthesis, and chemical intermediates. With a purity of ≥95%, it serves as a key reagent in the preparation of heterocyclic compounds, Schiff bases, and other bioactive molecules. The dihydrochloride salt form enhances stability and solubility in aqueous solutions, making it suitable for controlled reactions. Store in a cool, dry place away from light and moisture to maintain integrity. Ideal for researchers and scientists requiring precise and reliable building blocks for drug discovery and medicinal chemistry applications.
Properties
- CAS Number: 412327-07-2
- Complexity: 100
- IUPAC Name: (4-methoxyphenyl)methylhydrazine;dihydrochloride
- InChI: InChI=1S/C8H12N2O.2ClH/c1-11-8-4-2-7(3-5-8)6-10-9;;/h2-5,10H,6,9H2,1H3;2*1H
- InChI Key: XMPHUNHAMDBTBE-UHFFFAOYSA-N
- Exact Mass: 224.0483185
- Molecular Formula: C8H14Cl2N2O
- Molecular Weight: 225.11
- SMILES: COC1=CC=C(C=C1)CNN.Cl.Cl
- Topological: 47.3
- Monoisotopic Mass: 224.0483185
- Synonyms: 412327-07-2, (4-METHOXYBENZYL)HYDRAZINE DIHYDROCHLORIDE, 4-Methoxybenzylhydrazine dihydrochloride, [(4-methoxyphenyl)methyl]hydrazine dihydrochloride, (4-methoxybenzyl)hydrazine 2hcl, (4-methoxyphenyl)methylhydrazine;dihydrochloride, (4-Methoxybenzyl)hydrazine diHCl, Hydrazine, [(4-methoxyphenyl)methyl]-, dihydrochloride, MFCD06800897, 4-Methoxybenzylhydrazine diHCl, SCHEMBL2491984, XMPHUNHAMDBTBE-UHFFFAOYSA-N, BCP02652, BCP34601, AKOS015844914, Hydrazine,[(4-methoxyphenyl)methyl]-, SB10049, Hydrazine,p-methoxybenzyl-,hydrochloride, AS-50506, DA-39196, FM177072, 1-(4-methoxybenzyl)hydrazine hydrochloride, CS-0053733, (4-Methoxyphenyl)methylhydrazine dihydrochloride, P10418, (4-Methoxybenzyl)hydrazine dihydrochloride;1-(4-Methoxybenzyl)hydrazine dihydrochloride
(4-Methoxybenzyl)hydrazine dihydrochloride is primarily employed as a versatile intermediate in synthetic organic chemistry, particularly for constructing hydrazone linkages and heterocyclic scaffolds. It is widely used in pharmaceutical development for the synthesis of potential therapeutic agents, including antimicrobial and anticancer compounds. Researchers also utilize it in coupling reactions and as a precursor for Schiff base formation in coordination chemistry. Its stability and reactivity make it suitable for controlled functionalization in complex molecular architectures.
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