3-Iodo-4-methoxybenzoic Acid TCI I0959

Chemical Identity

CAS No.: 68507-19-7
PubChem: CID 624158·SID 253661117
Formula: C8H7IO3
Molecular weight: 278.04 g/mol
Purity: >97.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-iodo-4-methoxybenzoic acid
SMILES: COC1=C(C=C(C=C1)C(=O)O)I
InChIKey: HNJSYSWRPCCSQI-UHFFFAOYSA-N

Rp 1.565.550,00

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3-Iodo-4-methoxybenzoic Acid is a chemical compound widely used in organic laboratory reactions. It serves as a versatile building block in the synthesis of various organic compounds, particularly in non-heterocyclic chemistry. This compound is commonly utilized in research settings where controlled reactivity and structural stability are essential. Its presence in chemical experiments contributes to the development of new materials, pharmaceuticals, and functional chemicals. Due to its chemical versatility, it is a key component in many synthetic pathways.

The compound's unique structure, featuring an iodine atom and a methoxy group, makes it a preferred choice for chemists. The iodine group enhances its reactivity, allowing it to participate in nucleophilic and electrophilic reactions. The methoxy group adds polarity, influencing solubility and reaction behavior. These properties make it suitable for a wide range of synthetic applications. Its stability under controlled conditions ensures consistent results in laboratory experiments.

In Indonesian laboratories, 3-Iodo-4-methoxybenzoic Acid is a common reagent used in both academic and industrial research. It is frequently employed in the synthesis of bioactive compounds and pharmaceutical intermediates. Its availability in the local market supports ongoing research efforts in chemical sciences, enabling scientists to conduct experiments with reliable and accessible materials.

TCI brochures (PDF)

Iodinated Phenol／Benzoic Acid／Benzaldehyde Building Blocks 2024-11-15 · p. 2

Related TCI products

Organic synthesis of pharmaceutical intermediates due to its reactivity and structural versatility.
Reactions involving nucleophilic substitution because of the iodine atom's electrophilic nature.
Development of functional materials through controlled chemical modifications.
Research in bioactive compound synthesis due to its polar and reactive properties.
Industrial chemical production as a building block for various chemical derivatives.

Brand	TCI
CAS number	68507-19-7
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
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 light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactive nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize inhalation risks. It should not be stored near incompatible substances like strong oxidizers or acids. Regular inspection of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.

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