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Undeca-4,8-dione is an organic compound with the molecular formula C11H20O2. It is a diketone, which means it contains two carbonyl groups (C=O) in its structure. The carbon atoms in the molecule are numbered from 1 to 11, with the carbonyl groups located at positions 4 and 8. Undeca-4,8-dione is a colorless liquid with a mild, sweet odor. It is used in the synthesis of various chemicals, including fragrances and pharmaceuticals, due to its unique chemical properties and reactivity.

13505-35-6

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13505-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13505-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,0 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13505-35:
(7*1)+(6*3)+(5*5)+(4*0)+(3*5)+(2*3)+(1*5)=76
76 % 10 = 6
So 13505-35-6 is a valid CAS Registry Number.

13505-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name undecane-4,8-dione

1.2 Other means of identification

Product number -
Other names 4,8-Undecanedione

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:13505-35-6 SDS

13505-35-6Downstream Products

13505-35-6Relevant academic research and scientific papers

Long-range stereo-relay: Relative and absolute configuration of 1,n-glycols from circular dichroism of liposomal porphyrin esters

MacMillan, John B.,Molinski, Tadeusz F.

, p. 9944 - 9945 (2007/10/03)

The relative and absolute configurations of long-chain syn- and anti-1,5-, 1,7- and 1,9-glycols were determined from exciton-coupled circular dichroism (ECCD) of the corresponding bis-5-(4′-carboxyl)-5,10,15,20-tetraphenylporphyrin esters measured in uniform (φ = 26 nm), unilamellar liposomes. Long-range transmission of configuration by ECCD is made possible through partial ordering of glycol ester-lipid molecules by liposomal bilayers. Copyright

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