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1725-04-8

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1725-04-8 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 103, p. 5183, 1981 DOI: 10.1021/ja00407a039Tetrahedron Letters, 22, p. 1737, 1981 DOI: 10.1016/S0040-4039(01)90426-5

Check Digit Verification of cas no

The CAS Registry Mumber 1725-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1725-04:
(6*1)+(5*7)+(4*2)+(3*5)+(2*0)+(1*4)=68
68 % 10 = 8
So 1725-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O2/c14-13-11-9-7-5-3-1-2-4-6-8-10-12-15-13/h1-12H2

1725-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name oxacyclotetradecan-2-one

1.2 Other means of identification

Product number -
Other names 2-oxacyclotetradecan-1-one

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:1725-04-8 SDS

1725-04-8Relevant articles and documents

Flow Chemistry under Extreme Conditions: Synthesis of Macrocycles with Musklike Olfactoric Properties

Seemann, Alexandra,Panten, Johannes,Kirschning, Andreas

supporting information, p. 13924 - 13933 (2021/05/29)

Starting from small cyclic ketones, continuous flow synthesis is used to produce medium-sized rings and macrocycles that are relevant for the fragrance industry. Triperoxides are important intermediates in this process and are pyrolyzed at temperatures above 250 °C. The synthesis is carried out in two continuously operated flow reactors connected by a membrane-operated separator. The practicality of flow chemistry is impressively demonstrated in this work by the use of hazardous reagent mixtures (30% H2O2, 65% HNO3) and the pyrolysis of no less problematic peroxides. All new macrocycles were tested for their olfactory properties in relation to musk.

LACTONISIERUNG VON MAKROLID-SECOSAEUREN MIT "PUSH-PULL ACETYLENEN"

Gais, H.-J.

, p. 273 - 276 (2007/10/02)

A highly efficient method for the macrolactonization of seco-acids is described.Seco-acids are converted into stable enolesters 3 by the acetylene 1, which are cyclized under proton or Lewis acid catalysis.This new method has been successfully applied to the lactonization of the 7-epi-brefeldin A seco-acids 8a, b.

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