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15498-31-4

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15498-31-4 Usage

General Description

1,4-Dioxecane-5,10-dione, also known as 1,4-Cyclohexadiene-1,3-dione, is a chemical compound with the molecular formula C6H6O4. It is a cyclic diketone that is commonly used as a building block in the synthesis of various pharmaceuticals and organic compounds. 1,4-Dioxecane-5,10-dione is an important intermediate in the production of a wide range of drugs, including antibiotics, antifungals, and antiparasitic agents. It is also used as a precursor in the production of polymers and as a reagent in organic chemistry reactions. 1,4-Dioxecane-5,10-dione has potential applications in the field of medicine, materials science, and chemical synthesis. However, it is important to handle 1,4-Dioxecane-5,10-dione with caution due to its potential health hazards and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 15498-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,9 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15498-31:
(7*1)+(6*5)+(5*4)+(4*9)+(3*8)+(2*3)+(1*1)=124
124 % 10 = 4
So 15498-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O4/c9-7-3-1-2-4-8(10)12-6-5-11-7/h1-6H2

15498-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Dioxecane-5,10-dione

1.2 Other means of identification

Product number -
Other names dioxa-1,8 cyclodecane-dione-2,7

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:15498-31-4 SDS

15498-31-4Downstream Products

15498-31-4Relevant articles and documents

Does diatomic sulfur (S2) react as a free species?

Steliou, Kosta,Salama, Paul,Yu, Xiaoping

, p. 1456 - 1462 (2007/10/02)

A detailed study into the design and synthesis of stable 1,2-dithietane derivatives for the generation of diatomic sulfur (S2) was undertaken. Computer-aided evaluation of enthalpic differences was used to direct the synthesis of target compounds and, although all of the compounds calculated to afford S2 that were prepared did yield diatomic sulfur, an isolable 1,2-dithietane other than dithiatopazine failed to materialize. The results of this study provide convincing evidence that the computational procedure outlined can be successfully used to predict the course of S2 extrusion pathways from potential dithionocarbonylated derivatives. To determine if the disulfide moiety found in the Diels-Alder adduct derived from the addition of diatomic sulfur to conjugated 1,3-dienes is due to a transference mechanism involving the transient 1,2-dithietane intermediate, a chiral nonracemic binaphthyl source of S2 was prepared. Reactions of S2 from this source with chiral nonracemic and prochiral conjugated 1,3-dienes indicate that the added disulfide moiety would be inconsistent with a transference mechanism and that a "free" acting S2 unit is more likely to be involved.

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