Cas no 1446093-00-0 (Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1))

Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) is a specialized organic compound featuring a hydroxylamine moiety linked to a 4-iodobenzyl group, with a hydrochloride salt form enhancing stability and solubility. This reagent is particularly valuable in synthetic chemistry for its role as a versatile intermediate in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. The presence of the iodine substituent offers opportunities for further functionalization via cross-coupling reactions, while the hydroxylamine group enables participation in oxime or nitrone formation. Its crystalline solid form ensures convenient handling and storage. Suitable for controlled reactions, this compound is often employed in research and industrial applications requiring precise molecular modifications.
Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) structure
1446093-00-0 structure
Product Name:Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1)
CAS No:1446093-00-0
MF:C7H9ClINO
MW:285.509933233261
MDL:MFCD28125672
CID:5160711
Update Time:2025-06-11

Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) Chemical and Physical Properties

Names and Identifiers

    • Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1)
    • MDL: MFCD28125672
    • Inchi: 1S/C7H8INO.ClH/c8-7-3-1-6(2-4-7)5-10-9;/h1-4H,5,9H2;1H
    • InChI Key: QKTGWFUBZHRJRK-UHFFFAOYSA-N
    • SMILES: C(C1C=CC(I)=CC=1)ON.Cl

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Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) Related Literature

Additional information on Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1)

Comprehensive Overview of Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) (CAS No. 1446093-00-0)

Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) (CAS No. 1446093-00-0) is a specialized organic compound with significant applications in pharmaceutical research and chemical synthesis. This compound, often referred to as a hydroxylamine derivative, is characterized by its unique molecular structure, which includes an iodophenyl group. Its hydrochloride salt form enhances stability and solubility, making it a valuable reagent in modern laboratories.

The growing interest in hydroxylamine derivatives is driven by their role in the development of novel therapeutic agents. Researchers frequently search for "hydroxylamine derivatives in drug discovery" or "CAS 1446093-00-0 applications," highlighting its relevance in medicinal chemistry. This compound is particularly noted for its potential in targeted drug delivery systems and as a building block for bioactive molecules.

In synthetic chemistry, Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) is utilized for its ability to introduce functional groups into complex molecules. Its iodophenyl moiety offers opportunities for further modifications, such as cross-coupling reactions, which are pivotal in creating advanced materials. Queries like "iodophenyl compounds in synthesis" or "hydroxylamine reagents for organic chemistry" reflect its importance in this field.

From an analytical perspective, the compound's purity and stability are critical for reproducible results. Laboratories often inquire about "CAS 1446093-00-0 purity standards" or "handling hydroxylamine derivatives safely," emphasizing the need for high-quality reagents. Proper storage conditions, such as protection from light and moisture, are essential to maintain its efficacy.

The environmental and regulatory aspects of Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) are also of interest. While it is not classified as a hazardous material, responsible disposal and adherence to local regulations are recommended. Searches like "eco-friendly hydroxylamine derivatives" or "sustainable chemical synthesis" align with the increasing focus on green chemistry.

In summary, Hydroxylamine, O-[(4-iodophenyl)methyl]-, hydrochloride (1:1) (CAS No. 1446093-00-0) is a versatile compound with broad applications in drug development and organic synthesis. Its unique properties and adaptability make it a subject of ongoing research, as evidenced by trending searches such as "innovative uses of hydroxylamine derivatives" and "CAS 1446093-00-0 in pharmaceuticals."

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