5'-Chloro-3-hydroxy-2'-methyl-2-naphthanilide TCI C2102

Chemical Identity

Other names: N-(5-Chloro-o-tolyl)-3-hydroxy-2-naphthamide · Naphthol AS-KB · Azoic Coupling Component 21 · 5'-Chloro-N-(3-hydroxy-2-naphthoyl)-o-toluidine
CAS No.: 135-63-7
PubChem: CID 67275·SID 87559053
Formula: C18H14ClNO2
Molecular weight: 311.77 g/mol
Purity: >96.0%(N)
Reference databases: ChEBI·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: N-(5-chloro-2-methylphenyl)-3-hydroxynaphthalene-2-carboxamide
SMILES: CC1=C(C=C(C=C1)Cl)NC(=O)C2=CC3=CC=CC=C3C=C2O
InChIKey: XZOACPDZZYNJER-UHFFFAOYSA-N
MDL: MDL00021636

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5'-Chloro-3-hydroxy-2'-methyl-2-naphthanilide is a chemical compound widely used in organic synthesis reactions within laboratory settings. As a building block, it plays a crucial role in the development of complex molecular structures. This compound is commonly found in the synthesis of various compounds, including pharmaceuticals, dyes, and industrial chemicals. Its versatility makes it an essential material for researchers aiming to create new chemical entities.

The compound's aromatic structure provides stability, while the presence of hydroxyl and chloro groups enhances its reactivity. These functional groups allow for controlled manipulation in different chemical conditions, making it ideal for substitution reactions and other synthetic processes. Its chemical stability and reactivity make it a preferred choice for chemists working on compound development and modification.

In Indonesian laboratories, 5'-Chloro-3-hydroxy-2'-methyl-2-naphthanilide is utilized in organic chemistry research, particularly in the synthesis of bioactive compounds. It is frequently used in academic and research institutions to explore new synthetic techniques and expand knowledge in chemical sciences. Its application supports the development of new materials and pharmaceuticals, contributing to scientific innovation in the region.

Related TCI products

Synthesis of bioactive compounds for pharmaceutical development due to its reactivity and structural versatility.
Aromatic substitution reactions where stable core structures are required for further functionalization.
Organic chemistry research focused on creating new chemical entities with tailored properties.
Development of industrial dyes and pigments through controlled chemical modifications.
Exploration of novel synthetic pathways in academic and research laboratories for chemical innovation.

Brand	TCI
CAS number	135-63-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Ensure that storage areas are well-ventilated to minimize any potential risk of inhalation. Avoid contact with incompatible materials to maintain chemical stability. Regular monitoring of storage conditions ensures the integrity and safety of the compound in laboratory settings.

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