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4179-43-5

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4179-43-5 Usage

General Description

2-Furannonanoic acid, 5-pentyl- is a chemical compound with the molecular formula C10H16O3. It is a derivative of furan with a pentyl side chain. 2-Furannonanoic acid, 5-pentyl- is a carboxylic acid, which means it contains a functional group consisting of a carbon atom double bonded to an oxygen atom and also bonded to a hydroxyl group. 2-Furannonanoic acid, 5-pentyl- is primarily used in organic synthesis and as a building block for the production of various pharmaceuticals, agrochemicals, and flavors. It is also known for its potential anti-inflammatory and analgesic properties, making it a subject of interest in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 4179-43-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,7 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4179-43:
(6*4)+(5*1)+(4*7)+(3*9)+(2*4)+(1*3)=95
95 % 10 = 5
So 4179-43-5 is a valid CAS Registry Number.

4179-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(5-pentylfuran-2-yl)nonanoic acid

1.2 Other means of identification

Product number -
Other names 2-Furannonanoic acid,5-pentyl

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:4179-43-5 SDS

4179-43-5Downstream Products

4179-43-5Relevant articles and documents

Evaluation of the Cytotoxic Activity of Chiral (E)-13-Hydroxy-10-oxo-11-octadecenoic Acid and Its Lactone

Hayashi, Yoshiki,Nishikawa, Yasushi,Mori, Hirotaka,Matsushita, Yoh-ichi,Sugamoto, Kazuhiro,Matsui, Takanao

, p. 1771 - 1773 (1998)

Both the S and R enantiomers of (E)-13-hydroxy-10-oxo-11-octadecenoic acid (1) and (E)-10-oxo-11-octadecen-13-olide (2) had similar IC50 values against P388 mouse leukemia cells; i.e. the stereochemistry of the asymmetric center of 1 and 2 had no influence on the cytotoxic activity. Bioassay results of various compounds related to 1 and 2 suggests that the 1O-oxo and lactone moieties of 2 were important for enhancing the cytotoxicity. - Keywords: corn; cytotoxicity; fatty acid; (E)-13-hydroxy-10-oxo-11octadecenoic acid; (E)-10-oxo-11-octadecen-13-olide.

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