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7-Oxa-1,13-tridecanediol is a chemical compound with the molecular formula C9H18O3. It is a diol, which means it contains two hydroxyl (-OH) groups. The compound is characterized by a 13-carbon chain with an oxygen atom in the 7th position, forming an ether linkage. This structure gives it unique properties and potential applications in various chemical processes. It is an organic compound that can be used in the synthesis of other chemicals, pharmaceuticals, or as a building block in the creation of more complex molecules. The specific uses and properties of 7-oxa-1,13-tridecanediol would depend on the context in which it is being applied, and further research or technical data would be required to detail its specific applications and characteristics.

7259-78-1

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7259-78-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7259-78-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7259-78:
(6*7)+(5*2)+(4*5)+(3*9)+(2*7)+(1*8)=121
121 % 10 = 1
So 7259-78-1 is a valid CAS Registry Number.

7259-78-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-oxa-1,13-tridecanediol

1.2 Other means of identification

Product number -
Other names bis-(6-hydroxy-hexyl)-ether

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:7259-78-1 SDS

7259-78-1Downstream Products

7259-78-1Relevant academic research and scientific papers

PROCESS FOR PREPARING ε- EPSILON-CAPROLACTONE AND 1,6- HEXANEDIOL

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Page/Page column 19-21, (2012/04/10)

The invention relates to processes for preparing 1,6-hexanediol and very pure ε-caprolactone from a dicarboxylic acid solution (DCS), comprising the steps of (a) esterification of the DCS with alcohols, (b) partial catalytic hydrogenation of the esters, (c) distillative removal of 1,6- hexanediol and low boilers as the top product, and (d) cyclization of the 6-hydroxycaproic ester present in the bottoms fraction in the presence of a higher-boiling alcohol than caprolactone.

Regioselective and stereoselective cyclizations of chloropolyols in water: Rapid synthesis of hydroxytetrahydrofurans

Kang, Baldip,Chang, Stanley,Decker, Shannon,Britton, Robert

supporting information; body text, p. 1716 - 1719 (2010/09/05)

A concise, stereoselective synthesis of functionalized tetrahydrofuranols has been developed that involves heating readily available chloropolyols in water. These reactions are operationally straightforward and chemoselective for the formation of tetrahydrofurans, obviating the need for complicated protecting group strategies. The efficiency of this process is demonstrated in a short asymmetric synthesis of the natural product (+)-goniothalesdiol.

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