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CAS 16375-88-5

N-[4-(Hydroxymethyl)phenyl]acetamide TCI H1605

N-[4-(Hydroxymethyl)phenyl]acetamide TCI H1605

Chemical Identity

CAS No.
16375-88-5
PubChem
CID 152141·SID 354335075
Formula
C9H11NO2
Molecular weight
165.19 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N-[4-(hydroxymethyl)phenyl]acetamide
SMILES
CC(=O)NC1=CC=C(C=C1)CO
InChIKey
XEYORFKUJZEQCH-UHFFFAOYSA-N
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N-[4-(Hydroxymethyl)phenyl]acetamide is a chemical compound widely used as a building block in organic synthesis. This versatile reagent plays a crucial role in laboratories by enabling the construction of complex molecular structures. Its ability to participate in various chemical reactions makes it an essential component for researchers working on the development of bioactive compounds. Due to its stability and controlled reactivity, it is a preferred choice for a wide range of chemical experiments and research applications.

The compound’s chemical properties, including its amide and hydroxyl functional groups, contribute to its reactivity in substitution, redox, and condensation reactions. These characteristics make it suitable for use in environments where controlled chemical transformations are required. Its stability under normal laboratory conditions ensures that it remains effective throughout the experimental process. Additionally, its predictable behavior in different chemical environments enhances its reliability as a research tool.

In Indonesian laboratories, N-[4-(Hydroxymethyl)phenyl]acetamide is commonly used in organic chemistry research, particularly in academic institutions and research centers. It is frequently employed in projects related to the synthesis of bioactive molecules, drug development, and structural chemistry studies. Its availability and reliability make it a standard reagent in both teaching and research laboratories across Indonesia.

  • Organic synthesis projects benefit from this compound's ability to form complex molecular structures through amide and hydroxyl group interactions.
  • Bioactive compound development relies on its reactivity in substitution and condensation reactions, aiding in the creation of pharmaceutical candidates.
  • Structural chemistry research utilizes its stable molecular framework for studying molecular interactions and reaction mechanisms.
  • Teaching laboratories use it to demonstrate fundamental organic reactions and functional group chemistry in undergraduate courses.
  • Research institutions incorporate it into drug discovery programs to explore new synthetic pathways and molecular scaffolds.

Brand TCI
CAS number 16375-88-5
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply options
Physical form Solid or powder, depending on packaging
Storage Store in a cool, dry place away from direct sunlight and moisture

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its reactivity. Suitable storage containers include glass or high-density polyethylene (HDPE) bottles with airtight lids. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Avoid contact with incompatible materials, and ensure proper ventilation when working with this substance. Regular monitoring of storage conditions helps maintain the integrity of the compound for reliable experimental results.

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