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7,7'-Dibromo-3,3',4,4'-tetrahydro-2H,2H'-8,8'-bi-1,4-benzoazine is a heterocyclic chemical compound with a complex molecular structure. It is a tetrahydro-2H,2H'-8,8'-bi-1,4-benzoazine derivative with two bromine atoms attached to the 7th and 7th' positions. 7,7'-Dibromo-3,3',4,4'-tetrahydro-2H,2H'-8,8'-bi-1,4benzoazine features two fused benzene rings and exhibits potent inhibitory activity against the enzyme topoisomerase II.

781626-08-2

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    Cas No: 781626-08-2

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781626-08-2 Usage

Uses

Used in Pharmaceutical Industry:
7,7'-Dibromo-3,3',4,4'-tetrahydro-2H,2H'-8,8'-bi-1,4-benzoazine is used as a potential lead compound for the development of antitumor and antiviral agents due to its ability to inhibit topoisomerase II enzyme activity. This makes it a promising candidate for the treatment of various cancers and viral infections.
Used in Organic Synthesis:
7,7'-Dibromo-3,3',4,4'-tetrahydro-2H,2H'-8,8'-bi-1,4-benzoazine is used as a building block in the synthesis of organic and medicinal compounds. Its unique molecular structure and promising biological activity make it a valuable component in the creation of new and innovative pharmaceuticals and organic materials.

Check Digit Verification of cas no

The CAS Registry Mumber 781626-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,1,6,2 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 781626-08:
(8*7)+(7*8)+(6*1)+(5*6)+(4*2)+(3*6)+(2*0)+(1*8)=182
182 % 10 = 2
So 781626-08-2 is a valid CAS Registry Number.

781626-08-2Upstream product

781626-08-2Relevant articles and documents

AMINE-SUBSTITUTED DIPHENYLDIPHOSPHINES

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Page/Page column 48, (2008/06/13)

The invention relates to the 1,1'-diphenyl-2,2'-diphosphines of formulae (Ia), (Ib), having at least one amine substituent in para position to the phosphine group. These novel compounds are ligands for metal complexes that are catalysts for asymmetric addition reactions of prochiral organic compounds and whose catalytic properties can be adjusted in a substrate-specific manner via the substitution of the amino group.

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