(3-Bromophenyl)(mesityl)iodonium Trifluoromethanesulfonate TCI B5277

Chemical Identity

CAS No.: 1203709-76-5
PubChem: CID 44550063·SID 468590568
Formula: C16H15BrF3IO3S
Molecular weight: 551.2 g/mol
Purity: >98.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (3-bromophenyl)-(2,4,6-trimethylphenyl)iodanium;trifluoromethanesulfonate
SMILES: CC1=CC(=C(C(=C1)C)[I+]C2=CC=CC(=C2)Br)C.C(F)(F)(F)S(=O)(=O)[O-]
InChIKey: QTQFCDQRJRJUAN-UHFFFAOYSA-M

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(3-Bromophenyl)(mesityl)iodonium trifluoromethanesulfonate is a synthetic reagent widely used in organic chemistry laboratories. It belongs to the class of hypervalent iodine compounds, which are known for their unique reactivity and utility in various synthetic transformations. This compound serves as an efficient initiator in reactions that require iodine activation, making it a valuable tool for chemists working on complex molecule synthesis. Its role in promoting nucleophilic substitution reactions is particularly significant, allowing for the formation of structurally diverse organic compounds.

The compound is prized for its chemical stability and high reactivity towards a wide range of organic substrates. Its ability to act as a reliable iodine source enhances the efficiency of synthetic pathways, especially in reactions where precise control over reactivity is essential. The trifluoromethanesulfonate group further contributes to its stability and reactivity, making it a preferred choice for researchers aiming to achieve high yields and selectivity in their experiments.

In Indonesian laboratories, this reagent is commonly used in organic synthesis research, particularly in the development of complex molecules and reactions that require iodine activation. Its versatility and effectiveness make it a staple in chemical research, supporting both academic and industrial applications in the field of synthetic chemistry.

TCI brochures (PDF)

Hypervalent Iodine Compounds 2025-06-12 · p. 6

Related TCI products

Organic synthesis reactions where iodine activation is required for efficient nucleophilic substitution processes.
Development of complex organic molecules through controlled and selective chemical transformations.
Research in medicinal chemistry for the synthesis of bioactive compounds with specific structural features.
Catalytic systems that benefit from the high reactivity and stability of hypervalent iodine compounds.
Analytical chemistry applications involving the preparation of standard reagents for qualitative and quantitative analysis.

Brand	TCI
CAS number	1203709-76-5
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > Hypervalent Iodine Compounds
Pack sizes	Available in various quantities as per standard laboratory supply formats
Physical form	Solid or liquid, depending on the specific formulation
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 to maintain its chemical stability. It is recommended to use airtight containers made of materials compatible with its chemical nature, such as glass or high-density polyethylene. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment. In laboratory settings, it is important to ensure good ventilation and to avoid contact with incompatible substances. Proper labeling and storage conditions are essential to prevent accidental exposure and to maintain the integrity of the compound during use.

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