6788-84-7 Usage
General Description
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. 1,2-dioxetane is often used as a chemical intermediate in the synthesis of various organic compounds and pharmaceuticals, and it is also employed as a chemiluminescent reagent in the detection of biological molecules and in bioimaging applications. 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. When 1,2-dioxetane undergoes decomposition, it releases energy in the form of light, making it valuable for chemiluminescence-based assays and detection 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
6788-84-7Relevant articles and documents
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.
