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5-Heptyl-5-hydroxy-3,4-dimethylfuran-2(5H)-one is a complex organic compound with the molecular formula C13H22O3. It is a derivative of furan-2(5H)-one, featuring a five-carbon heptyl chain and two methyl groups attached to the third and fourth carbon atoms of the furan ring. The compound also has a hydroxyl group at the fifth position, which contributes to its polarity and potential reactivity. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as a building block in the creation of bio-based materials. Its unique structure and properties make it an interesting target for researchers in the field of organic chemistry and green chemistry.

6066-55-3

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6066-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6066-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6066-55:
(6*6)+(5*0)+(4*6)+(3*6)+(2*5)+(1*5)=93
93 % 10 = 3
So 6066-55-3 is a valid CAS Registry Number.

6066-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-heptyl-5-hydroxy-3,4-dimethylfuran-2-one

1.2 Other means of identification

Product number -
Other names 5-Heptyl-5-hydroxy-3.4-dimethyl-2.5-dihydro-furan-2-on

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:6066-55-3 SDS

6066-55-3Downstream Products

6066-55-3Relevant academic research and scientific papers

α,β-Unsaturated γ-lactones correlations between lipophilicity and biological activity

Dal Pozzo,Dansi,Biassoni

, p. 877 - 882 (2007/10/12)

A homogeneous series of α,β-unsaturated γ-lactones was prepared. Their in vitro activity against various microorganisms was quantitatively correlated, with the Hansch approach, to their lipophilicity, expressed by Rm chromatographic values. Although all the experimental results show a parabolic dependence, only in few cases the parabolic model calculated by Hansch fits to them. In most cases it was possible to find a good fitting between the ascending side of the parabola and the equation of Hansch. The meaning of the results and their utilization for future work are discussed.

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