70419-07-7

Basic information

• Product Name: (R)-(-)-2-NONANOL
• Synonyms: (R)-(-)-2-NONANOL;(R)-2-NONANOL;(R)-2-DECANOL;(R)-(-)-2-NONANOL, 97% (98% EE/GLC);(R)-1-Methyl-1-octanol;(R)-Nonan-2-ol
• CAS NO: 70419-07-7
• Molecular Formula: C₉H₂₀O
• Molecular Weight: 144.25
• Product Categories: Alcohols;Chiral Building Blocks;Organic Building Blocks
• Mol File: 70419-07-7.mol
• Article Data: 29

Chemical Properties

• Melting Point: 50-53 °C(lit.)
• Boiling Point: 195.5 °C at 760 mmHg
• Flash Point: >230 °F
• Appearance: /
• Density: 0.824 g/cm³
• Vapor Pressure: 0.108mmHg at 25°C
• Refractive Index: 1.43
• CAS DataBase Reference: (R)-(-)-2-NONANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(-)-2-NONANOL(70419-07-7)
• EPA Substance Registry System: (R)-(-)-2-NONANOL(70419-07-7)

Safety Data

• Safety Statements: 24/25
• WGK Germany: 3
• Hazardous Substances Data: 70419-07-7(Hazardous Substances Data)

Usage

General Description

(R)-(-)-2-Nonanol, also known as (R)-2-hydroxynonane, is a chiral compound with a nine-carbon chain and a hydroxyl group attached to the second carbon. It is a clear, colorless liquid with a mild, fatty odor. This chemical is commonly used as a flavoring agent in the food industry, as well as an ingredient in perfumes and personal care products due to its pleasant scent. It is also used in the production of surfactants, lubricants, and plasticizers. Additionally, (R)-(-)-2-Nonanol has been studied for its potential medical applications, including its antimicrobial, anti-inflammatory, and antiviral properties.

InChI:InChI=1/C9H20O/c1-3-4-5-6-7-8-9(2)10/h9-10H,3-8H2,1-2H3/t9-/m1/s1

Upstream product

• 821-55-6 2-Nonanone 
• 124-13-0 Octanal 
• 2371-70-2 tetramethyl titanium 
• 70419-06-6 (S)-nonan-2-ol 
• 544-97-8 dimethyl zinc(II) 
• 628-99-9 nonan-2-ol 
• 108-05-4 vinyl acetate 
• 124-07-2 Octanoic acid 
• 64-19-7 acetic acid 
• 142-62-1 hexanoic acid 
• 107-92-6 butyric acid 
• 14936-66-4 2-nonanyl acetate 
• 69727-42-0 2-nonyl butanoate 
• 55193-16-3 2-nonyl hexanoate 

Downstream Products

• 479629-72-6 (R)-1-methyloctyl-4-acetoxyphenylcarboxylate 
• 1346758-49-3 (S)-(+)-1-methyloctyl 3,5-dibromobenzoate 
• 1414963-58-8 (S)-trimethyl((4-(nonan-2-yloxy)phenyl)ethynyl)silane 
• 1414963-60-2 (S)-1-ethynyl-4-(nonan-2-yloxy)benzene 
• 1414963-63-5 (S)-4-((4-(nonan-2-yloxy)phenyl)ethynyl)phenol 
• 1414963-72-6 C₃₂H₄₆O₂ 
• 1414963-55-5 (S)-1-iodo-4-(nonan-2-yloxy)benzene 
• 1414963-66-8 C₂₃H₃₆O 
• 1414963-69-1 C₂₃H₂₈O 
• 1359079-02-9 (R)-(-)-1-methyloctyl p-toluenesulfonate 

Relevant articles and documents

Catalytic enantioselective addition of methyltriisopropoxititanium to aldehydes

An efficient catalyst for the enantioselective synthesis of chiral methyl carbinols from aldehydes is presented. The system uses methyltriisopropoxytitanium as a nucleophile and a readily available binaphthyl derivative as a chiral ligand. The enantioselective methylation of both aromatic and aliphatic aldehydes proceeds with good yields and high enantioselectivities under mild conditions.

ALKANE OXIDATION BY MODIFIED HYDROXYLASES

This invention relates to modified hydroxylases. The invention further relates to cells expressing such modified hydroxylases and methods of producing hydroxylated alkanes by contacting a suitable substrate with such cells.

Identification of key residues in Debaryomyces hansenii carbonyl reductase for highly productive preparation of (S)-aryl halohydrins

Key residues of Debaryomyces hansenii carbonyl reductase in the determination of the reducing activity towards aryl haloketones were identified through combinatorial mutation of conserved residues. This study provides a green and efficient biocatalyst for the synthesis of (S)-aryl halohydrins.