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CAS 936-02-7

Salicyl Hydrazide TCI S0242

Salicyl Hydrazide TCI S0242

Chemical Identity

CAS No.
936-02-7
PubChem
CID 13637·SID 87575775
Formula
C7H8N2O2
Molecular weight
152.15 g/mol
Purity
>98.0%(HPLC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-hydroxybenzohydrazide
SMILES
C1=CC=C(C(=C1)C(=O)NN)O
InChIKey
XSXYESVZDBAKKT-UHFFFAOYSA-N
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Salicyl Hydrazide is a chemical compound widely used in various chemical reactions and organic synthesis processes. As a fundamental building block in chemistry, it plays a crucial role in the formation of heterocyclic compounds and complex molecular structures. In laboratory settings, it functions as a reagent in condensation, substitution, and hydrazination reactions. Its reactivity allows it to combine with different functional groups, making it a valuable material for the synthesis of new compounds.

The compound's reactive nature is primarily due to its hydrazide group and phenyl group, which contribute to its high reactivity. The hydrazide group is particularly sensitive to reaction conditions, enabling the formation of a wide range of molecular structures and functionalities. This characteristic makes it a preferred choice in chemical applications, especially in the synthesis of bioactive compounds. Its stability under certain conditions also facilitates its handling and storage in laboratory environments.

In Indonesian laboratories, Salicyl Hydrazide is commonly used in research and development activities focused on organic chemistry. It is an essential component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its versatility and reactivity make it a go-to material for scientists and researchers working on complex chemical transformations and functional group modifications.

  • Organic synthesis for the creation of heterocyclic compounds due to its reactive hydrazide group.
  • Condensation reactions where it acts as a nucleophile to form new carbon-nitrogen bonds.
  • Substitution reactions for replacing functional groups in aromatic rings with hydrazide functionalities.
  • Hydrazination processes to introduce hydrazide moieties into organic molecules.
  • Bioactive compound development as a precursor in the synthesis of pharmaceutical and agrochemical products.

Brand TCI
CAS number 936-02-7
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 powder
Storage Store in a cool, dry place away from moisture and direct sunlight

Salicyl Hydrazide should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture and air. Due to its reactive nature, it should be handled in a well-ventilated area, preferably with appropriate personal protective equipment. Avoid contact with strong oxidizing agents or reactive metals. It is important to ensure that storage conditions remain consistent to preserve its chemical integrity and ensure safe usage in laboratory settings.

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