103962-05-6 4-(Trifluoromethoxy)iodobenzen

103962-05-6 4-(Trifluoromethoxy)iodobenzen Introduction

We are a pharmaceutical intermediate manufacturer of 4-(Trifluoromethoxy)iodobenzen.

Its CAS No. is 103962-05-6

Our pharmaceutical intermediates can be used in a variety of APIs.

103962-05-6 4-(Trifluoromethoxy)iodobenzen Specifications

103962-05-6 4-(Trifluoromethoxy)iodobenzen Factory display

Office Environment

Laboratory

Workshop/Warehouse

103962-05-6 4-(Trifluoromethoxy)iodobenzen Certification

Certificate

103962-05-6 4-(Trifluoromethoxy)iodobenzen FAQ

1. Manufacturer or trading company for 103962-05-6 4-(Trifluoromethoxy)iodobenzen?

4-(Trifluoromethoxy)iodobenzen is produced by EASTFINE , and we are in charge of overseas selling . Not just trading compamy .

2. 103962-05-6 4-(Trifluoromethoxy)iodobenzen supplier and factories or wholesale locates in such countries like?

China,America,Brazil,England,Russia,Poland,India,Pakistan,NewZealand,Korea,Australia,Dubai,Turkey,Indonesia,UAE.

3. Can I get a sample for trying 103962-05-6 4-(Trifluoromethoxy)iodobenzen?

yes , you can have 1 4-(Trifluoromethoxy)iodobenzen sample for starting the business , but it is not free

4. What the MOQ of 103962-05-6 4-(Trifluoromethoxy)iodobenzen?

please contact sale team for detail .

5. What is 4-(Trifluoromethoxy)iodobenzene?

4-(Trifluoromethoxy)iodobenzene (CAS 103962-05-6) is an aromatic compound with the molecular formula C₇H₄F₃IO. It features an iodine substituent and trifluoromethoxy group in para-position on a benzene ring, serving as a versatile building block in synthetic chemistry.

6. What are the physical characteristics of this compound?

This compound appears as a colorless to pale yellow liquid at room temperature. It has a molecular weight of 291.01 g/mol, boiling point of approximately 210-215°C, and density around 1.9 g/cm³. The compound is soluble in common organic solvents but insoluble in water.

7. How should this chemical be stored and handled?

For optimal stability, store in amber glass bottles under inert atmosphere (nitrogen or argon) at temperatures below 25°C. The container should be tightly sealed and protected from light exposure. Handling should occur in a fume hood with standard PPE including nitrile gloves and safety goggles.

8. What are the primary applications of this reagent?

This compound is particularly valuable for:

• Palladium-catalyzed cross-coupling reactions (Suzuki, Heck, Sonogashira)

• Nucleophilic aromatic substitutions

• Preparation of liquid crystals and electronic materials

• Pharmaceutical intermediate synthesis

9. What safety precautions are necessary?

The compound may cause skin and eye irritation. Avoid inhalation of vapors and direct contact. In case of exposure, flush affected areas with copious water and seek medical attention if irritation persists. Always review the material safety data sheet before use.

10. How is the purity typically verified?

Quality assessment includes:

• GC or HPLC analysis (typically ≥97% purity)

• Iodine content verification

• ⊃1;H and ⊃1;⁹F NMR spectroscopy

• Refractive index measurement (n20/D ~1.52)

11. What makes this compound chemically unique?

The combination of strong electron-withdrawing trifluoromethoxy group and excellent leaving group (iodine) creates exceptional reactivity in:

• Electrophilic aromatic substitutions

• Metal-halogen exchange reactions

• Radical reactions The iodine atom shows particular utility in transition metal-catalyzed processes.

12. Where can this compound be sourced?

This specialty chemical is available through fine chemical suppliers in various quantities. Standard packaging includes 1g, 5g, 25g, and 100g options, with custom quantities available for industrial-scale applications. Many suppliers provide technical support for application development.