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2-Octanoylfuran is a chemical compound with the molecular formula C12H18O2. It is a derivative of furan, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one oxygen atom. In 2-Octanoylfuran, an octanoyl group (a saturated fatty acid chain with eight carbon atoms) is attached to the 2-position of the furan ring. 2-Octanoylfuran is known for its unique aroma and is used in the fragrance industry to create various scent profiles. It is also found in some natural products and can be used as a flavoring agent in food and beverages. Due to its chemical structure, 2-Octanoylfuran exhibits properties such as low water solubility and high boiling point, making it suitable for use in a range of applications.

5456-77-9

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5456-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5456-77-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5456-77:
(6*5)+(5*4)+(4*5)+(3*6)+(2*7)+(1*7)=109
109 % 10 = 9
So 5456-77-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H18O2/c1-2-3-4-5-6-8-11(13)12-9-7-10-14-12/h7,9-10H,2-6,8H2,1H3

5456-77-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(furan-2-yl)octan-1-one

1.2 Other means of identification

Product number -
Other names 2-Octanoylfuran

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:5456-77-9 SDS

5456-77-9Downstream Products

5456-77-9Relevant academic research and scientific papers

A FACILE ROUTE TO 5-ALKYL-2(3H)-FURANONES BY PHOTOISOMERISATION OF ENEDICARBONYL COMPOUNDS

Auria, M. D',Mico, A. De,Piancatelly, G.,Scettry, A.

, p. 1661 - 1666 (2007/10/02)

A new and useful synthesis of a title compounds is reported.They can be obtained easily by photocyclization of enedicarbonyl compounds 3 and 4.A different behaviour, ascribed to the geometry of a double bond, is observed; 3 are converted only to butenolides 5, while trans-isomers 4 are converted into alkyl-furyl-ketones 5 and 6.A possible mechanism is described.

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