17701-32-5

Basic information

• Product Name: 2,2-DIMETHYLOCTANOYL CHLORIDE
• Synonyms: 2,2-DIMETHYLOCTANOYL CHLORIDE
• CAS NO: 17701-32-5
• Molecular Formula: C₁₀H₁₉ClO
• Molecular Weight: 190.7103
• Mol File: 17701-32-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 217.3°Cat760mmHg
• Flash Point: 79.5°C
• Appearance: /
• Density: 0.943g/cm³
• Vapor Pressure: 0.134mmHg at 25°C
• Refractive Index: 1.439
• CAS DataBase Reference: 2,2-DIMETHYLOCTANOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-DIMETHYLOCTANOYL CHLORIDE(17701-32-5)
• EPA Substance Registry System: 2,2-DIMETHYLOCTANOYL CHLORIDE(17701-32-5)

Safety Data

• Hazardous Substances Data: 17701-32-5(Hazardous Substances Data)

Usage

General Description

2,2-Dimethyloctanoyl chloride is an organic chemical compound with the molecular formula C10H19ClO. It is a clear, colorless liquid with a pungent odor, and is commonly used as a reagent in organic synthesis and chemical research. 2,2-DIMETHYLOCTANOYL CHLORIDE is an acyl chloride, meaning it contains a functional group consisting of a carbonyl group (C=O) bonded to a chlorine atom. It is a highly reactive compound and is often utilized in the production of various organic compounds, including pharmaceuticals, agrochemicals, and polymers. Due to its reactivity and potential hazards, 2,2-Dimethyloctanoyl chloride should be handled with care and appropriate safety precautions.

InChI:InChI=1/C10H19ClO/c1-4-5-6-7-8-10(2,3)9(11)12/h4-8H2,1-3H3

Upstream product

• 638-45-9 1-Iodohexane 
• 79-31-2 isobutyric Acid 
• 29662-90-6 dimethyloctanoic acid 

Downstream Products

• 103906-30-5 2,2-dimethyloctanamide 
• 25228-51-7 2,2-Dimethyl-octanoic acid [3-(2,2-dimethyl-octanoylamino)-phenyl]-amide 
• 25228-50-6 2,2-Dimethyl-octanoic acid [3-(2,2-dimethyl-propionylamino)-phenyl]-amide 
• 5540-93-2 2,2-Dimethyl-octanoic acid (3-chloro-4-nitro-phenyl)-amide 
• 97725-04-7 2,2-dimethyl-octanoic acid anilide 
• 532986-15-5 N-[(1R)-2-hydroxy-1-phenylethyl]-2,2-dimethyloctanamide 

Relevant articles and documents

Skin (by machine translation)

PROBLEM TO BE SOLVED: To provide a skin external preparation which has an excellent moisture retention effect, and excellent feeling of use without stickiness and strain.SOLUTION: A skin external preparation contains a copolymer that essentially consists of: one or more constitutional units derived from a hydrophobic and acrylic ester-based monomer including one (meth)acryloyl group and a plurality of acyl groups having a specific branch structure; and one or more constitutional units derived from a specific and hydrophilic structural acrylic monomer. The copolymer may have other constitutional units.

Intramolecular insertions into unactivated C(sp3)-H bonds by oxidatively generated β-diketone-α-gold carbenes: Synthesis of cyclopentanones

Generation of reactive α-oxo gold carbene intermediates via gold-catalyzed oxidation of alkynes has become an increasing versatile strategy of replacing hazardous diazo carbonyl compounds with benign and readily available alkynes in the development of efficient synthetic methods. However, one of the hallmarks of metal carbene/carbenoid chemistry, i.e., insertion into an unactivated C(sp3)-H bond, has not be realized. This study reveals for the first time that this highly valuable transformation can be readily realized intramolecularly by oxidatively generated β-diketone-α-gold carbenes using ynones as substrates. Substrate conformation control via the Thorpe-Ingold effect is the key design feature that enables generally good to excellent efficiencies, and synthetically versatile cyclopentanones including spiro-, bridged, and fused bicyclic ones can be readily accessed.