33950-46-8

Basic information

• Product Name: 2,2-DIMETHYL-1-PHENYL-1,3-PROPANEDIOL, 9 7%
• Synonyms: 2,2-DIMETHYL-1-PHENYL-1,3-PROPANEDIOL, 9 7%;2,2-Dimethyl-1-phenylpropane-1,3-diol
• CAS NO: 33950-46-8
• Molecular Formula: C₁₁H₁₆O₂
• Molecular Weight: 180.24354
• Mol File: 33950-46-8.mol
• Article Data: 13

Chemical Properties

• Melting Point: 76-80 °C(lit.)
• Boiling Point: 286-287 °C(lit.)
• Flash Point: 153.2°C
• Appearance: /
• Density: 1.0044 (rough estimate)
• Vapor Pressure: 0.000131mmHg at 25°C
• Refractive Index: 1.5130 (estimate)
• CAS DataBase Reference: 2,2-DIMETHYL-1-PHENYL-1,3-PROPANEDIOL, 9 7%(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-DIMETHYL-1-PHENYL-1,3-PROPANEDIOL, 9 7%(33950-46-8)
• EPA Substance Registry System: 2,2-DIMETHYL-1-PHENYL-1,3-PROPANEDIOL, 9 7%(33950-46-8)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 33950-46-8(Hazardous Substances Data)

Usage

General Description

2,2-Dimethyl-1-phenyl-1,3-propanediol, 9 7% is a chemical compound with a molecular formula C12H18O2. It is a colorless liquid with a 97% concentration. 2,2-DIMETHYL-1-PHENYL-1,3-PROPANEDIOL, 9 7% is commonly used as an intermediate in the synthesis of pharmaceuticals, polymers, and other organic compounds. It is known for its ability to act as a chiral building block, and it is often used in the production of chiral drugs and fine chemicals. Additionally, it has applications in the production of fragrances, flavors, and other specialty chemicals. Overall, 2,2-Dimethyl-1-phenyl-1,3-propanediol, 9 7% is a versatile chemical with a wide range of industrial uses.

InChI:InChI=1/C11H16O2/c1-11(2,8-12)10(13)9-6-4-3-5-7-9/h3-7,10,12-13H,8H2,1-2H3

Upstream product

• 597-31-9 2,2-dimethyl-3-hydroxypropionaldehyde 
• 100-52-7 benzaldehyde 
• 78-84-2 isobutyraldehyde 
• 50-00-0 formaldehyd 
• 611-70-1 phenyl isopropyl ketone 
• 52178-65-1 ethyl 3-hydroxy-2,2-dimethyl-3-phenylpropanoate 
• 1750-74-9 2-benzoyl-2-methylpropanal 
• 6651-34-9 2-methyl-1-(trimethylsilyloxy)-1-propene 
• 598-26-5 dimethylketene 
• 25491-42-3 ethyl 2,2-dimethyl-3-oxo-3-phenylpropionate 

Downstream Products

• 121108-77-8 5,5-dimethyl-4-phenyl-1,3-dioxane 
• 768-49-0 (2-methyl-1-propenyl)-benzene 
• 611-70-1 phenyl isopropyl ketone 
• 101499-58-5 1,3-diacetoxy-2,2-dimethyl-1-phenyl-propane 
• 100612-73-5 3-acetoxy-2,2-dimethyl-1-phenyl-propan-1-one 
• 24632-19-7 3,3-dimethyl-2-phenyloxetane 
• 98675-02-6 2-chloro-5,5-dimethyl-4-phenyl-1,3,2-dioxaphosphorinane 2-oxide 
• 167031-87-0 3-methanesulfonyloxy-2,2-dimethyl-1-phenyl-1-propanol 
• 64-19-7 acetic acid 
• 65-85-0 benzoic acid 
• 515174-36-4 racemic 2H-2-oxo-5,5-dimethyl-4-phenyl-1,3,2-dioxaphosphorinane 
• 170640-34-3 2-chloro-5,5-dimethyl-4-phenyl-[1,3,2]dioxaphosphinane 2-sulfide 

Relevant articles and documents

Phosphinous Acid Platinum Complex as Robust Catalyst for Oxidation: Comparison with Palladium and Mechanistic Investigations

Secondary phosphine oxides proved to be effective preligands to stabilise a hydroxy-platinum based catalyst that allows the aerobic/anaerobic oxidation of challenging substrates. Kinetic comparisons showed that this system is more efficient and stable than previously reported similar palladium-based catalysts. A neutral platinum dimer bearing bridging hydroxy ligands has been isolated and fully characterised by X-ray diffraction and its involvement in the mechanism has been evidenced by mechanistic studies.

Optical enrichment in enzyme-catalyzed resolution of 1-aryl-2,2-dimethyl-1,3-propanediols

Novozym 435 efficiently catalyzed the chemo-, regio-, and enantioselective transesterification of 1-aryl-2,2-dimethyl-1,3-propanediols in different organic solvents with vinyl acetate as the acetyl donor at room temperature. This enzyme-catalyzed chemical

Synthesis and biological activity of a-hydroxyphosphonates

Ten α-hydroxyphosphates were synthesized and the preliminary bioessay indicated that these compounds exhibited certain herbicidal activities. Copyright Taylor & Francis Group, LLC.