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1,2-dioxetane is a highly reactive and unstable organic compound with the chemical formula C2H4O2. It is a cyclic ether and a type of dioxetane, characterized by its two oxygen atoms and four carbon atoms arranged in a ring structure. Due to its instability, 1,2-dioxetane is typically synthesized and used in situ, immediately before its intended application, to minimize the risk of decomposition.

6788-84-7

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6788-84-7 Usage

Uses

Used in Chemical Synthesis:
1,2-dioxetane is used as a chemical intermediate for the synthesis of various organic compounds and pharmaceuticals. Its reactivity allows for the formation of new chemical bonds and the creation of complex molecules.
Used in Chemiluminescent Reagents:
1,2-dioxetane is used as a chemiluminescent reagent in the detection of biological molecules and in bioimaging applications. When it undergoes decomposition, it releases energy in the form of light, making it valuable for chemiluminescence-based assays and detection methods.
Used in Bioimaging Applications:
1,2-dioxetane is used as a luminescent probe in bioimaging to visualize biological processes and structures. Its light emission upon decomposition allows researchers to track and monitor molecular interactions and cellular events in real-time.
Used in Environmental Monitoring:
1,2-dioxetane can be used as a sensitive and selective chemiluminescent indicator for detecting trace amounts of pollutants or contaminants in environmental samples. Its light emission upon interaction with specific analytes enables the development of rapid and reliable monitoring methods.
Used in Analytical Chemistry:
1,2-dioxetane is employed as a reagent in various analytical techniques, such as high-performance liquid chromatography (HPLC) and capillary electrophoresis (CE), to enhance the detection and quantification of target compounds. Its chemiluminescent properties provide increased sensitivity and selectivity in these analytical methods.

Check Digit Verification of cas no

The CAS Registry Mumber 6788-84-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6788-84:
(6*6)+(5*7)+(4*8)+(3*8)+(2*8)+(1*4)=147
147 % 10 = 7
So 6788-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C2H4O2/c1-2-4-3-1/h1-2H2

6788-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dioxetane

1.2 Other means of identification

Product number -
Other names 1,2-Dioxethan

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:6788-84-7 SDS

6788-84-7Downstream Products

6788-84-7Relevant academic research and scientific papers

EFFECTS OF METHYLATION ON THE THERMAL STABILITY AND CHEMILUMINESCENCE PROPERTIES OF 1,2-DIOXETANES.

Adam,Baader

, p. 410 - 416 (2007/10/22)

The unknown monomethyl derivative 1f and the parent 1,2-dioxetane 1g have been prepared and fully characterized. The influence of the degree and pattern of methyl substitution of the complete set of 1,2-dioxetanes 1a-g on the activation parameters ( DELTA H** DOUB DAG , DELTA S** DOUB DAG , and DELTA G** DOUB DAG ) and on the excitation yields ( phi **T and phi **S) have been determined. It was found that (1) the thermal stability increases with the degree of methylation, (2) the pattern of methylation does not alter appreciably thermal stability, (3) triplet n, pi * states are preferentially energized, and (4) the triplet and singlet excitation yields increase with the degree of methylation. These experimental results are compared with thermochemical estimates and rationalized in terms of the diradical hypothesis and energy surface crossings.

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