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Undecanoic acid, 11-oxo-, also known as 11-oxoundecanoic acid or 11-keto-undecanoic acid, is a chemical compound with the molecular formula C11H20O3. It is a derivative of undecanoic acid, featuring a ketone group (C=O) at the 11th carbon position. This organic compound is a colorless liquid with a slight odor and is soluble in organic solvents. It is used in the synthesis of various chemicals, pharmaceuticals, and fragrances, and can also be found as a minor component in some essential oils. Due to its reactivity, it is important to handle it with care, following proper safety protocols.

53163-99-8

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53163-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53163-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,6 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53163-99:
(7*5)+(6*3)+(5*1)+(4*6)+(3*3)+(2*9)+(1*9)=118
118 % 10 = 8
So 53163-99-8 is a valid CAS Registry Number.

53163-99-8SDS

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 11-oxoundecanoic acid

1.2 Other means of identification

Product number -
Other names 11-oxo-undecanoic 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:53163-99-8 SDS

53163-99-8Relevant academic research and scientific papers

cis/trans-Ozonides of Cycloolefins

Griesbaum, Karl,Ball, Volker,Beck, Johannes,McCullough, Kevin

, p. 1993 - 2000 (2007/10/03)

Ozonolyses in pentane of the unsubstituted cycloolefins having eleven-, twelve-, fourteen- and sixteen-membered rings (1b-e) and of cyclohexadecen-8-one (12) gave the corresponding cis- (2b-e; cis-15a) and trans-ozonides (3b-e; trans-15a), whereas cyclodecene (1a) gave only the corresponding cis-ozonide (2a).Ozonolyses on polyethylene of the dimethyl-substituted cycloolefins bearing fourteen- and sixteen-membered rings (7b,c) also afforded cis- and trans-isomeric ozonides (8, 9), whereas from the twelve-membered ring (7a) only the corresponding cis-ozonide (8a) was formed. - Keywords: Ozonides; Cycloolefins

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