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3,6-Diethyl-3,6-octane-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24459-12-9

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24459-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24459-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,5 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24459-12:
(7*2)+(6*4)+(5*4)+(4*5)+(3*9)+(2*1)+(1*2)=109
109 % 10 = 9
So 24459-12-9 is a valid CAS Registry Number.

24459-12-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-diethyloctane-3,6-diol

1.2 Other means of identification

Product number -
Other names 3,6-Octanediol,3,6-diethyl

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:24459-12-9 SDS

24459-12-9Downstream Products

24459-12-9Relevant academic research and scientific papers

Arene-promoted lithiation of 1,n-dihaloalkanes (n=2-6): a comparative study

Abou, Abdeslam,Foubelo, Francisco,Yus, Miguel

, p. 10417 - 10424 (2007/10/03)

The reaction of 1,n-dichloroalkanes 3a (n=2-6) with an excess of lithium powder and a catalytic amount of 4,4′-di-tert-butylbiphenyl (DTBB; 2.5 mol %) in the presence of different carbonyl compounds [ButCHO, PhCHO, Et2CO, (CH2/

TiCl4/Mg/BrCH2CH2Br Reagent System: A 1,2-Diorganometallic Equivalent

Rao, S. Achyutha,Periasamy, M.

, p. 1583 - 1586 (2007/10/02)

1,2-Diorganometallic species generated utilizing the TiCl4/Mg/BrCH2CH2/Br reagent system reacts with ketones to give the corresponding 1,4-diols and/or 1,2-diols in moderate yields.

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