14097-24-6

Basic information

• Product Name: 1,3-diphenylpropan-1-ol
• CAS NO: 14097-24-6
• Molecular Formula: C₁₅H₁₆O
• Molecular Weight: 212.2869
• Mol File: 14097-24-6.mol
• Article Data: 266

Chemical Properties

• Boiling Point: 344.9°C at 760 mmHg
• Flash Point: 144.6°C
• Density: 1.073g/cm³
• Vapor Pressure: 2.44E-05mmHg at 25°C
• Refractive Index: 1.587
• CAS DataBase Reference: 1,3-diphenylpropan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-diphenylpropan-1-ol(14097-24-6)
• EPA Substance Registry System: 1,3-diphenylpropan-1-ol(14097-24-6)

Safety Data

• Hazardous Substances Data: 14097-24-6(Hazardous Substances Data)

Usage

Physical state

White solid

Odor

Pleasant

Uses

a. Fragrance ingredient in perfumes and personal care products
b. Flavoring agent
c. Solvent in various industrial applications

Antimicrobial properties

Used in pharmaceutical and cosmetic products for preservative effects

Synthesis

Used in the synthesis of other organic compounds

Research applications

Potential applications in the field of organic chemistry research

Upstream product

• 120-46-7 1,3-diphenylpropanedione 
• 94-41-7 benzalacetophenone 
• 67-64-1 acetone 
• 56-23-5 tetrachloromethane 
• 98-86-2 acetophenone 
• 100-51-6 benzyl alcohol 
• 104-53-0 3-phenyl-propionaldehyde 
• 1078-58-6 diphenylzinc 
• 78-79-5 isoprene 
• 934-56-5 trimethyl(phenyl)stannane 
• 541-16-2 t-butyl malonate 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 15014-25-2 malonic acid dibenzyl ester 
• 105-53-3 diethyl malonate 

Downstream Products

• 3412-44-0 1,3-diphenylpropene 
• 1083-30-3 dihydrochalcone 
• 5209-18-7 cis-1,3-diphenylpropene 
• 3412-44-0 (1E)-1,3-diphenylpropene 
• 40028-03-3 1-chloro-1,3-diphenylpropane 
• 21460-80-0 (1-bromopropane-1,3-diyl)dibenzene 
• 1081-75-0 1,3-diphenylpropane 
• 26461-03-0 1-phenylindane 
• 14097-24-6 (R)-1,3-diphenylpropanol 
• 19120-36-6 phenyl-carbamic acid-(1,3-diphenyl-propyl ester) 
• 532984-16-0 (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid (1,3-diphenyl)-propyl ester 
• 1033079-96-7 C₁₈H₁₈F₃NO₂ 
• 6624-04-0 2-benzyl-1,3-diphenyl-propan-1-one 
• 24547-82-8 2-benzyl-1,3-diphenylpropan-1-ol 

Relevant articles and documents

Microwave-assisted solid reaction: Reduction of ketones using sodium borohydride

A general and efficient procedure for microwave-assisted reduction of liquid and solid ketones using sodium borohydride without solvents is described. The added support can enhance both the efficiency and chemoselectivity of reduction.

Nickel-catalysed three-component connection reaction of a phenyl group, conjugated dienes, and aldehydes: Stereoselective synthesis of (E)-5-phenyl-3-penten-1-ols and (E)-3-methyl-5-phenyl-3-penten-1-ols

In the presence of 10 mol% of Ni(acac)2, Ph2Zn reacts with 1,3-butadiene and aldehydes at room temperature to give 1-alkyl and 1-aryl substituted (E)-5-phenyl-3-penten-1-ols (3) in good yields. Under similar conditions, the three components of Ph3BZnEt2, isoprene, and aldehydes combine with each other to furnish 1-alkyl and 1-aryl substituted (E)-3-methyl-5-phenyl-3-penten-1-ols (5) in good yields.

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Asymmetric transfer hydrogenation of unsaturated ketones; factors influencing 1,4- vs 1,2- regio- and enantioselectivity, and alkene vs alkyne directing effects

A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of enones using Ru(II) catalysts. Electron-rich rings adjacent to the C[dbnd]O group reduce the level of C[dbnd]O reduction compared to C[dbnd]C. The ATH reaction can readily discriminate between double and triple bonds adjacent to ketones, reducing the double bond but leaving a triple bond intact in the major product.

Cobalt-Catalyzed Chemoselective Transfer Hydrogenative Cyclization Cascade of Enone-Tethered Aldehydes

The ligand-free Co-catalyzed chemoselective reductive cyclization cascade of enone-tethered aldehydes with i-PrOH as the environmentally benign hydrogen surrogate is developed by this study. Mechanistic studies disclosed that such a protocol is initiated