syn-2-Nitrobenzaldoxime [Deprotecting Agent] TCI N0486

Chemical Identity

CAS No.: 4836-00-4
PubChem: CID 5372068·SID 87573812
Formula: C7H6N2O3
Molecular weight: 166.13 g/mol
Purity: >85.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (NZ)-N-[(2-nitrophenyl)methylidene]hydroxylamine
SMILES: C1=CC=C(C(=C1)/C=N\O)[N+](=O)[O-]
InChIKey: IHMGDCCTWRRUDX-YVMONPNESA-N

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Syn-2-Nitrobenzaldoxime is a chemical compound used as a deprotecting agent in various organic chemical reactions. It plays a critical role in the deprotection process, which involves removing protective groups from organic molecules to enable further chemical reactions. This compound is widely utilized in laboratory settings for its ability to selectively and efficiently remove protecting groups without interfering with the integrity of the target molecule. Its application is particularly significant in the synthesis of complex organic compounds, especially in the formation of heterocyclic structures and other intricate molecular frameworks.

The compound is valued for its chemical stability and controlled reactivity, making it suitable for use under a variety of reaction conditions. It exhibits good solubility in organic solvents, which facilitates mixing and reaction processes in the laboratory. These properties ensure that it performs reliably without introducing unwanted side reactions or degrading the quality of the final product. Its predictable behavior and compatibility with different reaction systems make it a preferred choice for chemists working on complex synthetic pathways.

In Indonesian laboratories, Syn-2-Nitrobenzaldoxime is commonly used in organic chemistry research, particularly in the fields of pharmacology and the synthesis of bioactive compounds. It is a key reagent in the development of new compounds with potential medical or industrial applications. Many research institutions and universities in Indonesia rely on this compound to advance their studies in synthetic chemistry and drug discovery. Its consistent performance and reliability make it an essential tool in the laboratory environment.

Related TCI products

Organic Synthesis: Syn-2-Nitrobenzaldoxime is ideal for organic synthesis due to its ability to selectively remove protecting groups, enabling the formation of complex molecular structures without interference.
Heterocyclic Compound Formation: This compound is widely used in the synthesis of heterocyclic compounds because it facilitates the deprotection of functional groups, allowing for the creation of ring structures with high efficiency.
Bioactive Compound Development: It plays a vital role in the synthesis of bioactive compounds, supporting research in pharmacology and drug discovery by enabling the modification of molecular structures.
Complex Molecule Construction: Its controlled reactivity and solubility make it suitable for the construction of complex molecules, where precise deprotection is essential for achieving the desired chemical outcomes.
Research and Development: It is a preferred choice in research and development settings due to its reliability and compatibility with various reaction conditions, supporting innovation in chemical synthesis.

Brand	TCI
CAS number	4836-00-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid or liquid, depending on formulation
Storage	Store in a cool, dry place away from direct sunlight

Syn-2-Nitrobenzaldoxime should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Due to its chemical nature, it should be handled in a well-ventilated area or under a fume hood to minimize inhalation risks. Appropriate personal protective equipment, such as gloves and safety goggles, should be worn when handling this material. It is important to avoid contact with skin and eyes, and in case of accidental exposure, immediate rinsing with water is advised. Proper storage and handling procedures ensure the safety of laboratory personnel and the integrity of the compound.

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