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TCI

CAS 619-25-0

3-Nitrobenzyl Alcohol TCI N0178

3-Nitrobenzyl Alcohol TCI N0178

Chemical Identity

CAS No.
619-25-0
Formula
C7H7NO3
Molecular weight
153.14 g/mol
Purity
>97.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(3-nitrophenyl)methanol
SMILES
C1=CC(=CC(=C1)[N+](=O)[O-])CO
InChIKey
CWNPOQFCIIFQDM-UHFFFAOYSA-N
PubChem
CID 69267
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3-Nitrobenzyl Alcohol is a chemical compound widely used as a foundational material in various chemical reactions. It plays a crucial role in the synthesis of complex compounds, particularly in the fields of organic chemistry and pharmacology. In laboratory settings, this compound serves as a precursor for the creation of other substances with specific biological activities. Its reactivity makes it a valuable component in substitution and reduction reactions.

The compound’s molecular structure is stable yet highly reactive, making it ideal for reactions that require a nitro group-containing substrate. Its solubility in organic solvents simplifies processes such as separation and isolation in laboratory procedures. These properties contribute to its popularity among chemists and researchers. Additionally, its versatility allows it to be used in the synthesis of heterocyclic and aromatic compounds, which are essential in pharmaceutical and chemical research.

In Indonesian laboratories, 3-Nitrobenzyl Alcohol is commonly used in chemical and pharmaceutical research. It is frequently found in projects related to drug development, organic compound modification, and the study of aromatic reactivity. Its availability and ease of use make it a preferred choice for researchers seeking reliable and effective chemical building blocks.

  • Drug development research utilizes 3-Nitrobenzyl Alcohol for synthesizing compounds with targeted biological activities.
  • Organic synthesis projects benefit from its reactivity, allowing for the creation of complex molecules through substitution and reduction reactions.
  • Pharmaceutical studies often employ this compound in the modification of organic compounds to enhance therapeutic properties.
  • Aromatic reactivity research leverages its stable yet reactive nature to explore chemical behavior in various reaction conditions.
  • Compound isolation and purification processes take advantage of its solubility in organic solvents for efficient separation techniques.

Brand TCI
CAS number 619-25-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

3-Nitrobenzyl Alcohol should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air. Since it is a reactive chemical, it should be kept away from incompatible substances such as strong oxidizers. Proper labeling of storage containers is essential for safety and traceability. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. Regular monitoring of storage conditions ensures the compound remains suitable for use in chemical and pharmaceutical applications.

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