5454-71-7 Usage
Description
(2,3-dihydro-1-benzofuran-2-ylmethyl)(iodo)mercury, also known as Hg(OCOC7H7I), is an organomercury compound with the chemical formula C15H13HgIO2. It is composed of a benzofuran ring attached to a methyl group and an iodine atom, both of which are bonded to a mercury atom. (2,3-dihydro-1-benzofuran-2-ylmethyl)(iodo)mercury is known for its use in organic synthesis and as a catalyst in various chemical reactions.
Uses
Used in Organic Synthesis:
(2,3-dihydro-1-benzofuran-2-ylmethyl)(iodo)mercury is used as a reagent in organic synthesis for its ability to facilitate specific chemical reactions and transformations. Its unique structure allows it to participate in various organic synthesis processes, contributing to the formation of complex organic molecules.
Used as a Catalyst in Chemical Reactions:
In the chemical industry, (2,3-dihydro-1-benzofuran-2-ylmethyl)(iodo)mercury is utilized as a catalyst to accelerate and enhance the efficiency of certain chemical reactions. Its catalytic properties enable it to lower the activation energy required for reactions to proceed, thereby increasing the reaction rate and improving overall process efficiency.
It is crucial to handle (2,3-dihydro-1-benzofuran-2-ylmethyl)(iodo)mercury with caution due to its toxicity. Proper management and safety measures are essential to minimize health risks associated with this organomercury compound.
Check Digit Verification of cas no
The CAS Registry Mumber 5454-71-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5454-71:
(6*5)+(5*4)+(4*5)+(3*4)+(2*7)+(1*1)=97
97 % 10 = 7
So 5454-71-7 is a valid CAS Registry Number.
5454-71-7Relevant articles and documents
Amino-and mercurio-substituted 4′,5'-dihydropsoralens and therapeutical uses thereof
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, (2008/06/13)
5′-substituted, 4′,5′-dihydropsoralen compounds (5) bearing tertiary amines (and salts thereof), quaternary ammonium moieties or organomercurial moieties are described. Also described are 2-substituted mercurimethyl-2-3-dihydro-benzofurans of forumla (7): Also reported are versatile direct syntheses through a hitherto unknown compounds such as 3-R-4,8-dimethyl-4′,5′-dihydro-5′-bromomethylpsoralen or a 3-R-4,8-dimethyl-4′, 5′-dihydro-5′-iodomethylpsoralen to prepare a structurally diverse array of partially reduced psoralens and benzofurans. The presence of a permanent ammonium charge in these psoralens precludes membrane passage and the mono-unsaturation precludes the cross-linking of nuclear DNA, thereby minimizing the mutagenic/carcinogenic side effects long associated with psoralen-derived therapies. The presence of a mercury functionality provides a reactive cell-binding group on these psoralens with unique cytotoxicity without light activation and an enhancement of cytotoxicity activity upon light activation. The invention also relates to These partially reduced and quaternized psoralens, amino-substituted psoralens, and mercurio psoralens display impressive pharmacology against PAM 212 keratinocytes, a model cell line employed as a test system to indicate epidermal cytotoxicity and cancer. The compounds of the invention also have antimicrobicidal activity useful in pharmacologic agents for mammals (e.g. the treatment of tuberculosis) as well as in controlling the growth of microorganisms on substrates and in aqueous systems.
