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7,8-Dioxabicyclo[4.2.0]octane, also known as 1,4-dioxane, is a cyclic ether with the chemical formula C4H8O2. It is a colorless, volatile, and highly flammable liquid with a sweet odor. This organic compound is commonly used as a solvent in various industrial processes, including the production of cellulose acetate, resins, and adhesives. Due to its ability to dissolve a wide range of organic compounds, it is also employed in the pharmaceutical and chemical industries. However, 1,4-dioxane has been classified as a probable human carcinogen by the International Agency for Research on Cancer (IARC), and its presence in consumer products and the environment has raised concerns due to its potential health risks.

278-47-7

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278-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 278-47-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 278-47:
(5*2)+(4*7)+(3*8)+(2*4)+(1*7)=77
77 % 10 = 7
So 278-47-7 is a valid CAS Registry Number.

278-47-7SDS

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 cyclohexene hydroperoxide

1.2 Other means of identification

Product number -
Other names cyclohexenyl peroxide

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:278-47-7 SDS

278-47-7Upstream product

278-47-7Downstream Products

278-47-7Relevant academic research and scientific papers

Epoxidation of olefins using O = VIV (L)/70percent TBHP system

Agarwal, D. D.,Rastogi, R.,Sangha, P. K.

, p. 254 - 256 (2007/10/02)

Epoxidation of olefins is catalysed by oxovanadium(IV) complexes using 70percent t-butylhydroperoxide (TBHP) as oxidant.Competitive epoxidation of cycloolefins follows the order: norbornene > cycloheptene > cyclohexene.EPR spectra show that the coordination of hydroperoxide to metal center takes place during epoxidation.

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