(2,2-Difluoro-1-methylethyl)benzene

Base Information

• Chemical Name: (2,2-Difluoro-1-methylethyl)benzene
• CAS No.: 57514-09-7
• Molecular Formula: C9H10F2
• Molecular Weight: 156.175
• Hs Code.: 2903999090
• Mol file: 57514-09-7.mol

Synonyms:1,1-Difluor-2-phenylpropan;(2,2-Difluoro-1-methylethyl)benzene;(1,1-difluoropropan-2-yl)benzene;1,1-difluoro-2-phenylpropane;

Chemical Property of (2,2-Difluoro-1-methylethyl)benzene

Chemical Property:

• Boiling Point: 159.438 °C at 760 mmHg
• Flash Point: 38.508 °C
• PSA: 0.00000
• Density: 1.036g/cm³
• LogP: 3.05520

Purity/Quality:

97% ^*data from raw suppliers

(2,2-Difluoro-1-methylethyl)benzene 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: (2,2-Difluoro-1-methylethyl)benzene, a chemical compound, finds various applications across different fields. In the realm of organic synthesis, it serves as a valuable building block for producing complex molecules due to its unique structural features. In the field of materials science, (2,2-Difluoro-1-methylethyl)benzene can be used in the formulation of specialty polymers and resins, contributing to the development of advanced coatings, adhesives, and plastics with enhanced properties. Additionally, (2,2-Difluoro-1-methylethyl)benzene may have applications in the fragrance and flavor industry, where it can be utilized as a constituent for creating specific scents and tastes. Its versatility in both organic chemistry and materials science underscores its importance in various industrial processes and innovations.

Technology Process of (2,2-Difluoro-1-methylethyl)benzene

There total 8 articles about (2,2-Difluoro-1-methylethyl)benzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

α-(difluoromethyl)styrene (345-60-8) → 2,2-difluoro-1-methylethylbenzene (57514-09-7)

Guidance literature:

With palladium on activated charcoal; hydrogen; In methanol; at 20 ℃; for 3h;

DOI:10.1039/c7cc04377e

Reference yield: 59.0%

Trifluoro-methanesulfonic acid 2-phenyl-1-trifluoromethanesulfonyloxy-propyl ester (141694-58-8) → 2,2-difluoro-1-methylethylbenzene (57514-09-7)

Guidance literature:

With tetra-n-butylammonium difluorotriphenylstannate; In dichloromethane; for 8h; Ambient temperature;

DOI:10.1016/0040-4039(93)88046-L

Reference yield:

2-Phenylpropanal (34713-70-7) → 2,2-difluoro-1-methylethylbenzene (57514-09-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 63 percent

2: 59 percent / tetrabutylammonium difluorotriphenylstannate / CH₂Cl₂ / 8 h / Ambient temperature

With tetra-n-butylammonium difluorotriphenylstannate; In dichloromethane;

DOI:10.1016/0040-4039(93)88046-L

upstream raw materials:

1-propenylbenzene

α-(Chlorodifluoromethyl)styrene

Trifluoro-methanesulfonic acid 2-phenyl-1-trifluoromethanesulfonyloxy-propyl ester

2-Phenylpropanal

Downstream raw materials:

C₉H₁₀F₂O₃S

4-(1,1-difluoropropan-2-yl)benzenesulfonyl chloride

2-(1,1-difluoropropan-2-yI)benzene-1-sulfonyl chloride