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3-Undecenoic acid is a naturally occurring organic compound found in various plants, particularly in the castor bean plant (Ricinus communis). It is a saturated monocarboxylic acid with a 10-carbon chain and a double bond at the third carbon atom, giving it the chemical formula C11H20O2. 3-Undecenoic acid has been studied for its potential antimicrobial properties, particularly against fungi and some bacteria. It is also used in the production of certain pharmaceuticals and has been investigated for its potential applications in the treatment of certain skin conditions. The acid is known for its ability to disrupt the cell membrane of microorganisms, leading to their death, which is why it has garnered interest in the field of natural antimicrobial agents.

4189-01-9

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4189-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4189-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4189-01:
(6*4)+(5*1)+(4*8)+(3*9)+(2*0)+(1*1)=89
89 % 10 = 9
So 4189-01-9 is a valid CAS Registry Number.

4189-01-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name undec-3-enoic acid

1.2 Other means of identification

Product number -
Other names 3-Undecenoic acid

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:4189-01-9 SDS

4189-01-9Downstream Products

4189-01-9Relevant academic research and scientific papers

Practical synthesis of (E)-α,β-unsaturated carboxylic acids using a one-pot hydroformylation/decarboxylative Knoevenagel reaction sequence

Kemme, Susanne T.,?mejkal, Tomá?,Breita, Bernhard

supporting information; experimental part, p. 989 - 994 (2009/05/27)

Combining the regioselective room temperature/ambient pressure hydroformylation and a modification of the Doebner-Knoevenagel reaction allowed for the development of an efficient, one-pot procedure for the synthesis of (E)-α,β-unsaturated carboxylic acids. The reaction proceeds under mild conditions, tolerates a variety of functional groups and gives (E)-α,β-unsaturated carboxylic acids in good yields and with excellent regio-and stereocontrol. The practicability of this process has been demonstrated by a short protecting group-free synthesis of the queen honeybee pheromones 9-ODA[( E)-9-oxodec-2-enoic acid] and 9-HDA[( E)-9-hydroxydec-2-enoic acid].

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