20389-01-9 Usage
Description
2,6-DIIODO-P-BENZOQUINONE, also known as 2,6-diiodo-1,4-benzoquinone, is a chemical compound characterized by its molecular formula C6H2I2O2. This dark brown solid is soluble in organic solvents and is recognized for its potential applications in various industries.
Uses
Used in Organic Synthesis:
2,6-DIIODO-P-BENZOQUINONE is utilized as a reagent in organic synthesis for the production of a wide range of other organic compounds. Its unique chemical properties make it a valuable component in creating diverse chemical structures.
Used in Dye Production:
In the dye industry, 2,6-DIIODO-P-BENZOQUINONE is employed as a key component in the manufacturing process. Its chemical structure contributes to the development of various dye products.
Used in Pharmaceutical Production:
The pharmaceutical industry leverages 2,6-DIIODO-P-BENZOQUINONE in the development and synthesis of different medicinal compounds. Its role in creating new pharmaceuticals highlights its versatility in chemical applications.
Used in Anti-Tumor Applications:
2,6-DIIODO-P-BENZOQUINONE has been studied for its potential use in anti-tumor applications, indicating its possible role in the medical field for combating cancer.
Used in Anti-Microbial Applications:
Similarly, this chemical compound has been investigated for its anti-microbial properties, suggesting its potential use in products designed to inhibit microbial growth.
It is crucial to handle 2,6-DIIODO-P-BENZOQUINONE with care due to its harmful nature if ingested or inhaled, and its potential to cause skin and eye irritation upon contact.
Check Digit Verification of cas no
The CAS Registry Mumber 20389-01-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,8 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20389-01:
(7*2)+(6*0)+(5*3)+(4*8)+(3*9)+(2*0)+(1*1)=89
89 % 10 = 9
So 20389-01-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H2I2O2/c7-4-1-3(9)2-5(8)6(4)10/h1-2H
20389-01-9Relevant articles and documents
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Kvalnes
, p. 670 (1934)
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A concise synthesis of thyroxine (T4) and 3,5,3'-Triiodo-L-thyronine (T3)
Salamonczyk, Grzegorz M.,Oza, Vibha B.,Sih, Charles J.
, p. 6965 - 6968 (2007/10/03)
The mono- and di-iodo derivatives of 1-oxaspiro[2,5]bicycloocta-4,7-dien-6-one, 8 and 9, reacted readily with 3,5-diiodo-L-tyrosine at pH 8.0 to give 3,5,3'-triiodo-L-thyronine (T3) and thyroxine in 70% and 94% yields respectively. In turn, 8 and 9 were prepared by the sodium bismuthate oxidation of their corresponding iodinated p-hydroxybenzyl alcohol derivatives, 6 and 7 in 32% and 37% yields.
