53685-77-1 Usage
Description
4-Heptadecanone is a long-chain ketone commonly found in foods and plants, characterized by its clear, colorless liquid form and a subtle floral scent.
Used in Food and Beverage Industry:
4-Heptadecanone is used as a flavoring agent and aroma compound for enhancing the taste and smell of various food and beverage products.
Used in Perfumery and Aromatherapy:
4-Heptadecanone is used as a key ingredient in essential oils derived from flowers such as roses and jasmine, contributing to their distinct fragrances and therapeutic properties.
Used in Pesticide and Insect Repellent Development:
4-Heptadecanone is used as an active ingredient in the development of insect repellents and pesticides due to its potential insecticidal properties.
Used in Antibacterial Applications:
4-Heptadecanone is used as an antibacterial agent in various studies, demonstrating its potential to inhibit the growth of certain bacteria.
Check Digit Verification of cas no
The CAS Registry Mumber 53685-77-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,8 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53685-77:
(7*5)+(6*3)+(5*6)+(4*8)+(3*5)+(2*7)+(1*7)=151
151 % 10 = 1
So 53685-77-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H34O/c1-3-5-6-7-8-9-10-11-12-13-14-16-17(18)15-4-2/h3-16H2,1-2H3
53685-77-1Relevant articles and documents
A General Approach to Intermolecular Olefin Hydroacylation through Light-Induced HAT Initiation: An Efficient Synthesis of Long-Chain Aliphatic Ketones and Functionalized Fatty Acids
Guin, Joyram,Paul, Subhasis
supporting information, p. 4412 - 4419 (2021/02/05)
Herein, an operationally simple, environmentally benign and effective method for intermolecular radical hydroacylation of unactivated substrates by employing photo-induced hydrogen atom transfer (HAT) initiation is described. The use of commercially available and inexpensive photoinitiators (Ph2CO and NHPI) makes the process attractive. The olefin hydroacylation protocol applies to a wide array of substrates bearing numerous functional groups and many complex structural units. The reaction proves to be scalable (up to 5 g). Different functionalized fatty acids, petrochemicals and naturally occurring alkanes can be synthesized with this protocol. A radical chain mechanism is implicated in the process.