CAS 3001-15-8

4,4′-Diiodo-1,1′-biphenyl

Description:

4,4′-Diiodo-1,1′-biphenyl, with the CAS number 3001-15-8, is an organic compound characterized by the presence of two iodine atoms attached to the para positions of a biphenyl structure. This compound is a member of the biphenyl family, which consists of two phenyl rings connected by a single bond. The introduction of iodine substituents significantly influences its chemical properties, including increased molecular weight and altered electronic characteristics. 4,4′-Diiodo-1,1′-biphenyl is typically a solid at room temperature and may exhibit a crystalline structure. It is often used in organic synthesis and materials science, particularly in the development of organic semiconductors and as a precursor for various chemical reactions. The presence of iodine atoms can enhance the compound's reactivity and solubility in organic solvents. Additionally, due to its halogen content, it may exhibit interesting photophysical properties, making it a subject of study in fields such as organic electronics and photochemistry.

Formula: C₁₂H₈I₂

InChI: InChI=1/C12H8I2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8H

InChI key: InChIKey=GPYDMVZCPRONLW-UHFFFAOYSA-N

SMILES: IC1=CC=C(C=C1)C2=CC=C(I)C=C2

Synonyms:

• 1,1'-Biphenyl, 4,4'-diiodo-
• 1-Iodo-4-(4-iodophenyl)benzene
• 4,4'-Diiodo-1'-Biphenyl
• 4,4'-Diiodo-1,1'-biphenyl
• 4,4′-Diiododiphenyl
• Biphenyl, 4,4'-diiodo
• P,P'-Diiodobiphenyl
• 4,4-Diiodobiphenyl
• 4,4′-Diiodobiphenyl
• 4,4''-DIIODOBIPHENYL 98%
• 4,4'-diiidodiphenyl
• 4,4-DIIODOBIPHENYL 99.5%
• 4,4'-DIIODOBIPHENYL, TECH., 90%
• 4,4'-DIODOBIPHENYL
• 4-(4'-IODOPHENYL)IODOBENZENE
• 4,4'-Diiodobiphenyl (DIB)

4,4'-Diiodobiphenyl

CAS: 3001-15-8

Formula: C₁₂H₈I₂

Purity: >98.0%(GC)

Color and Shape: Light orange to Yellow to Green powder to crystal

Molecular weight: 406.00

Ref: 3B-D2315

4,4'-Diiodobiphenyl, 99%

CAS: 3001-15-8

4,4?-diiodobiphenyl was coupled with (trimethylsilyl) acetylene via a Sonogashira-Hagihara reaction to afford the (trimethylsilyl)ethynyl derivative. 4,4?-diiodobipheny enhanced the expression of the luciferase gene. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesa

Formula: C₁₂H₈I₂

Purity: 99%

Color and Shape: Pale yellow, Crystals or powder or crystalline powder

Molecular weight: 406.01

Ref: 02-B21970

4,4'-Diiodo-1,1'-biphenyl

CAS: 3001-15-8

Formula: C₁₂H₈I₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 406.0009

Ref: IN-DA003KDQ

4,4'-Diiodobiphenyl

CAS: 3001-15-8

4,4'-Diiodobiphenyl

Purity: 98%

Color and Shape: Powder

Molecular weight: 406.00g/mol

Ref: 54-OR6696

4,4''-Diiodobiphenyl

CAS: 3001-15-8

Formula: C₁₂H₈I₂

Molecular weight: 406.00

Ref: 7W-GK9153

4,4-Diiodobiphenyl

CAS: 3001-15-8

4,4-Diiodobiphenyl is a synthetic organic compound that is created by the iodination reaction of biphenyl. The sodium hydrogen reacts with copper oxide in the presence of hydrochloric acid to create 4,4-diiodobiphenyl. This product can be used as a precursor to metal carbonyls and is therefore important in the chemical industry. 4,4-Diiodobiphenyl can also be used to synthesize other organic compounds, including diphenyl ethers. The environmental risks associated with this compound are its toxic properties and its ability to pollute water supplies.

Formula: C₁₂H₈I₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 406 g/mol

Ref: 3D-FD13961

4,4′-Diiodobiphenyl

CAS: 3001-15-8

Formula: C₁₂H₈I₂

Purity: 95%+

Color and Shape: Solid, Beige powder

Molecular weight: 406.005

Ref: 10-F080260