1- (4-Iodophenyl) naphthalene

1- (4-Iodophenyl) naphthalene (CAS: 1001337-35-4) is an organic aromatic compound belonging to the naphthalene derivative family, characterized by a naphthalene skeleton with a 4-iodophenyl group substituted at the 1-position. Its molecular formula is C16H11I, with a molecular weight of 326.16. It is a stable crystalline solid with typical aromatic compound reactivity (such as Suzuki-Miyaura coupling, Heck reaction) and good thermal stability, and is widely used as a key intermediate in chemical synthesis, optoelectronic materials, pharmaceutical R&D and fine chemical manufacturing.

1- (4-Iodophenyl) naphthalene, 4- (1-Naphthyl) iodobenzene, 4-Iodo-1-naphthylbenzene, 1- (4-Iodophenyl) naphthalene, 4- (Naphthalen-1-yl) iodobenzene, 1- (p-Iodophenyl) naphthalene

1. Optoelectronic Material Intermediates: 1- (4-Iodophenyl) naphthalene (CAS: 1001337-35-4) is an important intermediate in the synthesis of organic optoelectronic materials, widely used in the preparation of organic light-emitting diodes (OLEDs) and organic semiconductors, as its naphthalene and iodophenyl conjugated structure enhances charge transport performance and luminous efficiency of the materials. 2. Pharmaceutical Intermediates: It is applied in the synthesis of pharmaceutical compounds, especially in the R&D and production of anti-tumor and anti-inflammatory drugs, relying on its aromatic structure and iodine-substituted functional group to provide key reactive sites for constructing complex drug molecular structures and improving drug efficacy. 3. Fine Chemical Intermediates: 1- (4-Iodophenyl) naphthalene (CAS: 1001337-35-4) serves as a key intermediate in the synthesis of fine chemicals such as organic catalysts, specialty dyes and corrosion inhibitors, providing a stable conjugated aromatic backbone for the final products to enhance their chemical and physical properties. 4. Chemical Research Reagents: It is widely used as a standard reagent and research tool in organic synthesis, materials chemistry and aromatic chemistry research, facilitating the study of reaction mechanisms of naphthalene derivatives and the development of new synthetic routes for conjugated aromatic compounds.

≥98%

C16H11I

326.16

Store in a cool, dry and well-ventilated place, away from heat, open flame and direct sunlight, sealed tightly to prevent moisture absorption and oxidation; keep away from strong oxidants and strong bases

2 years under proper storage

White to off-white crystalline powder, insoluble in water, soluble in organic solvents such as dichloromethane, chloroform, toluene and tetrahydrofuran (THF)

Reagent Grade, Industrial Grade

1.52 g/cm3