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2,2'-(4,6-dichloro-5-methoxy-1,3-phenylene)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1221589-79-2

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1221589-79-2 Usage

Type of compound

Complex organic compound

Structure

Bis(alkoxy)arylborane, containing two boron atoms attached to a central phenylene group

Functional groups

4,6-dichloro, 5-methoxy, 1,3-phenylene, 4,4,5,5-tetramethyl-1,3,2-dioxa

Uses

Organic synthesis, reagent in the formation of carbon-carbon and carbon-heteroatom bonds, development of pharmaceuticals and agrochemicals

Chemical reactivity

Participates in a variety of chemical reactions

Potential applications

Field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 1221589-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,5,8 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1221589-79:
(9*1)+(8*2)+(7*2)+(6*1)+(5*5)+(4*8)+(3*9)+(2*7)+(1*9)=152
152 % 10 = 2
So 1221589-79-2 is a valid CAS Registry Number.

1221589-79-2Relevant academic research and scientific papers

COMPOUNDS AND ANTI-TUMOR NQO1 SUBSTRATES

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, (2013/04/25)

Compounds of Formula (I) can be selectively lethal toward a variety of different cancer cell types. The compounds are useful for the management, treatment, control, or adjunct treatment of diseases, where the selective lethality is beneficial in chemotherapeutic therapy.

Chemistry and biology of deoxynyboquinone, a potent inducer of cancer cell death

Bair, Joseph S.,Palchaudhuri, Rahul,Hergenrother, Paul J.

supporting information; experimental part, p. 5469 - 5478 (2010/07/03)

Deoxynyboquinone (DNQ) is a potent antineoplastic agent with an unknown mechanism of action. Here we describe a facile synthetic route to this anthraquinone, and we use this material to determine the mechanism by which DNQ induces death in cancer cells. DNQ was synthesized in seven linear steps through a route employing three palladium-mediated coupling reactions. Experiments performed on cancer cells grown in hypoxia and normoxia strongly suggest that DNQ undergoes bioreduction to its semiquinone, which then is re-oxidized by molecular oxygen, forming superoxide that induces cell death. Furthermore, global transcript profiling of cells treated with DNQ shows elevation of transcripts related to oxidative stress, a result confirmed at the protein level by Western blotting. In contrast to most other antineoplastic agents that generate reactive oxygen species (ROS), DNQ potently induces death of cancer cells in culture, with IC50 values between 16 and 210 nM. In addition, unlike the experimental therapeutic elesclomol, DNQ is still able to induce cancer cell death under hypoxic conditions. This mechanistic understanding of DNQ will allow for a more comprehensive evaluation of the potential of direct ROS generation as an anticancer strategy, and DNQ itself has potential as a novel anticancer agent.

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