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3,5,8-Trimethylazuleno[6,5-b]furan is a complex organic compound characterized by a unique molecular structure that features an azulene core fused with a furan ring. The azulene moiety is a five-membered ring with alternating double bonds, and the furan ring is a heterocyclic structure containing one oxygen atom. The compound is further distinguished by the presence of three methyl groups attached at the 3rd, 5th, and 8th positions of the azulene ring. This specific arrangement of atoms and functional groups endows 3,5,8-trimethylazuleno[6,5-b]furan with distinct chemical properties and potential applications in various fields, such as materials science and pharmaceuticals, where its electronic and steric characteristics may be exploited.

489-79-2

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489-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 489-79-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 489-79:
(5*4)+(4*8)+(3*9)+(2*7)+(1*9)=102
102 % 10 = 2
So 489-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O/c1-9-4-5-12-10(2)6-15-14(7-13(9)12)11(3)8-16-15/h4-8H,1-3H3

489-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5,8-trimethylazuleno[6,5-b]furan

1.2 Other means of identification

Product number -
Other names Linderazulene

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:489-79-2 SDS

489-79-2Upstream product

489-79-2Downstream Products

489-79-2Relevant academic research and scientific papers

One-step synthesis of furan rings from α-isopropylidene ketones mediated by iodine/DMSO: An approach to potent bioactive terpenes

Salihila, Jonida,Silva, Lúcia,Pérez Del Pulgar, Helena,Quílez Molina, Ana,González-Coloma, Azucena,Olmeda, A. Sonia,Quílez Del Moral, José F.,Barrero, Alejandro F.

, p. 6886 - 6894 (2019/06/14)

The system I2/dimethyl sulfoxide mediates the one-step transformation of α-isopropylidene ketones into furan rings following a biomimetic approach. This methodology has been used for the synthesis of terpene furans such as mintfurane, curzerene, atractylon, and isoatractylon, all of them possessing interesting biological activities. The synthesis of linderazulene directly from 4,5-epoxygermacrone via a cascade reaction shows the potential of this protocol. Additionally, this compound proved to show significant ixodicidal activity.

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