87050-83-7 Usage
Uses
Used in Organic Synthesis:
2,2'-Ethylenebis(6-(bromomethyl)-4-benzoquinone) is used as a reagent for its ability to participate in redox reactions, which is crucial in the synthesis of various organic compounds.
Used in Dye Production:
2,2'-Ethylenebis(6-(bromomethyl)-4-benzoquinone) is utilized as a precursor in the production of dyes, where its chemical properties contribute to the formation of the desired colorants.
Used in Polymer Production:
2,2'-Ethylenebis(6-(bromomethyl)-4-benzoquinone) is employed in the synthesis of polymers, where its bromomethyl groups and redox activity play a role in the polymerization process.
Used in Pharmaceutical Manufacturing:
It is also used in the pharmaceutical industry, where its unique structure and reactivity are harnessed in the development of certain drugs.
Used in Chemical Compounds Synthesis:
Due to its bromomethyl groups, 2,2'-Ethylenebis(6-(bromomethyl)-4-benzoquinone) serves as a valuable precursor for the synthesis of a range of other chemical compounds, expanding its utility in the chemical industry.
Safety Note:
It is important to handle 2,2'-Ethylenebis(6-(bromomethyl)-4-benzoquinone) with care, as its bromomethyl groups can present health and safety hazards if not managed with appropriate safety measures.
Check Digit Verification of cas no
The CAS Registry Mumber 87050-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,5 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87050-83:
(7*8)+(6*7)+(5*0)+(4*5)+(3*0)+(2*8)+(1*3)=137
137 % 10 = 7
So 87050-83-7 is a valid CAS Registry Number.
87050-83-7Relevant academic research and scientific papers
Anti-cancer agents and processes for their preparation
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, (2008/06/13)
Compounds of the formula STR1 wherein R1 and R2 are either two hydrogen atoms or together form a methylene group, and each X is a bromo, iodo or tosyloxy group and the dotted bonds indicate that the central linkage is attached to the
Bis(bioreductive) alkylating agents: Synthesis and biological activity in a nude mouse human carcinoma model
Witiak, Donald T.,Kamat, Prabhakar L.,Allison, Debra L.,Liebowitz, Stephen M.,Glaser, Ronald,et al.
, p. 1679 - 1686 (2007/10/02)
Chemical investigations leading to the construction of bis(bioreductive) alkylating agents having both conformationally restricted and mobile spacer regions are described. Two targets having the conformationally mobile ethylene spacer group, namely, 2,2'-ethylenebis[6-(hydroxymethyl)-p-benzoquinone] diacetate (3b) and 2,2'-ethylenebis[6-(bromomethyl)-p-benzoquinone] (3c), were studied in vivo and in vitro using an established epithelial/Burkitt lymphoma hybrid cell line (D98/HR1) previously shown to induce carcinomas in nude mice. Inactivity of both test compounds in vitro, the relative resistance of these cells to test drugs in vitro, and the selective antitumor properties of the bis(bromomethyl) analogue in vivo lead to the proposal that this compound undergoes bioreduction to an alkylating species in the hypoxic core of the tumor, thereby exerting its action.
