112777-68-1

Basic information

• Product Name: (1R)-1-(3-Methylphenyl)-1-propanol
• Synonyms: (1R)-1-(3-Methylphenyl)-1-propanol;(R)-1-(3-tolyphenyl)-1-propanol
• CAS NO: 112777-68-1
• Molecular Formula: C₁₀H₁₄O
• Molecular Weight: 150.21756
• Mol File: 112777-68-1.mol
• Article Data: 58

Chemical Properties

• Boiling Point: 228.9±8.0 °C(Predicted)
• Appearance: /
• Density: 0.979±0.06 g/cm3(Predicted)
• PKA: 14.70±0.20(Predicted)
• CAS DataBase Reference: (1R)-1-(3-Methylphenyl)-1-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R)-1-(3-Methylphenyl)-1-propanol(112777-68-1)
• EPA Substance Registry System: (1R)-1-(3-Methylphenyl)-1-propanol(112777-68-1)

Safety Data

• Hazardous Substances Data: 112777-68-1(Hazardous Substances Data)

Usage

Description

(1R)-1-(3-Methylphenyl)-1-propanol, also known as alpha-ethyl-m-tolylmethanol, is a chemical compound with a molecular formula C10H14O. It is classified as an alcohol and is a colorless liquid with a faint floral odor.

Uses

Used in Fragrance Industry:
(1R)-1-(3-Methylphenyl)-1-propanol is used as a fragrance ingredient for its floral scent, contributing to the formulation of perfumes, soaps, and cosmetics.
Used in Flavor Industry:
(1R)-1-(3-Methylphenyl)-1-propanol is used as a flavoring agent to enhance the taste of food and beverages.
Used in Organic Synthesis:
(1R)-1-(3-Methylphenyl)-1-propanol has potential applications in organic synthesis, serving as a building block in the production of other chemical compounds.
Used in Chemical Production:
(1R)-1-(3-Methylphenyl)-1-propanol can be utilized as a building block in the production of various chemical compounds, expanding its applications across different industries.

Upstream product

• 557-20-0 diethylzinc 
• 620-23-5 m-tolyl aldehyde 
• 587-03-1 3-methylbenzyl alcohol 

Relevant articles and documents

New atropisomeric amino alcohol ligands for enantioselective addition of diethylzinc to aldehydes

Efficient synthesis of several new atropisomeric amino alcohols having 1-phenyl-1H-pyrrole skeleton are reported. Steric arrangements of the products were confirmed by a single-crystal X-ray measurement. The consequences of the size of the N-substituents

Binaphthyl-based chiral ligands: Design, synthesis and evaluation of their performance in enantioselective addition of diethylzinc to aromatic aldehydes

The design strategy and the performance of binaphthyl-based chiral ligands were evaluated with computation and enantioselective addition of diethylzinc to aromatic aldehydes. Under optimized conditions, enantioselective addition of diethylzinc to aromatic aldehydes provided the desired optically active secondary alcohols in high isolated yields (up to 91%) and excellent enantiomeric excesses (up to 98% ee).

Chiral P,N-ligands for the highly enantioselective addition of diethylzinc to aromatic aldehydes

A new sterically hindered chiral P,N-ligand was synthesized and successfully applied to copper catalyzed asymmetric addition of diethylzinc to aromatic aldehydes. Various aromatic aldehydes can react smoothly to give the corresponding addition products with good to excellent enantioselectivities, which provides a readily accessible method for the preparation of chiral secondary alcohols.