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TCI

CAS 618-49-5

3-Hydroxybenzamide TCI H1643

3-Hydroxybenzamide TCI H1643

Chemical Identity

CAS No.
618-49-5
PubChem
CID 342403·SID 468591978
Formula
C7H7NO2
Molecular weight
137.14 g/mol
Purity
>98.0%(HPLC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
3-hydroxybenzamide
SMILES
C1=CC(=CC(=C1)O)C(=O)N
InChIKey
NGMMGKYJUWYIIG-UHFFFAOYSA-N
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3-Hydroxybenzamide is a chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As a key building block in chemical reactions, it plays a vital role in organic chemistry by serving as a versatile reactant. Its presence in chemical laboratories is essential for the development of new compounds and the advancement of research in various scientific fields. This compound is commonly utilized in both academic and industrial research environments due to its reactivity and chemical stability.

One of the main reasons 3-Hydroxybenzamide is preferred in laboratory work is its favorable solubility in organic solvents and its predictable chemical behavior. These properties allow researchers to control reaction conditions effectively, making it suitable for a range of chemical transformations. Its moderate reactivity ensures that it can participate in various reactions such as esterification, amidation, and substitution without undergoing unwanted side reactions. This makes it an ideal choice for synthetic chemists seeking reliable and consistent results.

In Indonesian laboratories, 3-Hydroxybenzamide is frequently used in organic chemistry research and educational settings. It is a common reagent in university-level courses where students learn about molecular structures and reaction mechanisms. Its application extends to the synthesis of new compounds, supporting both teaching and research activities in the chemical sciences. The compound's reliability and versatility make it a valuable asset in the Indonesian scientific community.

  • Organic synthesis of complex molecules requiring a reactive and stable building block
  • Amidation reactions for the formation of amide bonds in organic compounds
  • Esterification processes to create ester derivatives from carboxylic acids
  • Substitution reactions where functional group modification is required
  • Educational experiments demonstrating molecular structure and chemical reactivity

Brand TCI
CAS number 618-49-5
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
Storage Store in a cool, dry place away from moisture and direct sunlight

3-Hydroxybenzamide should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical degradation. Avoid storing near incompatible substances such as strong acids or bases. Always ensure proper ventilation when handling the compound to minimize inhalation risks. General laboratory precautions include wearing appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling and prevent accidental contact.

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