81-44-7 Usage
Derivative of anthraquinone
Anthraquinone is a group of organic compounds used as dyes and pigments 1-Benzoyl氨基-4-溴代蒽醌 is a modified version of this group, inheriting its color properties.
Presence of benzoylamino group
A functional group consisting of a benzoyl (C6H5CO) and an amino group (NH2) This group contributes to the compound's chemical reactivity and properties.
Presence of bromine atom
A halogen element (Br) The bromine atom influences the compound's stability, color, and potential pharmaceutical properties.
Commonly used in production of dyes and pigments
Vibrant color and high stability The compound's chemical structure and properties make it suitable for creating stable, brightly colored dyes and pigments.
Potential pharmaceutical properties
Being studied for possible use in treating various medical conditions The unique structure and properties of 1-Benzoyl氨基-4-溴代蒽醌 may have therapeutic applications in the future.
Health hazards if not used properly
Requires careful handling Due to its chemical nature, 1-Benzoyl氨基-4-溴代蒽醌 may pose risks to human health if not handled or used according to safety guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 81-44-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81-44:
(4*8)+(3*1)+(2*4)+(1*4)=47
47 % 10 = 7
So 81-44-7 is a valid CAS Registry Number.
InChI:InChI=1/C21H12BrNO3/c22-15-10-11-16(23-21(26)12-6-2-1-3-7-12)18-17(15)19(24)13-8-4-5-9-14(13)20(18)25/h1-11H,(H,23,26)
81-44-7Relevant articles and documents
PREPARATION METHOD OF ORIGINAL DYE OF VAT BROWN R
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, (2012/12/13)
A preparation method of original dye of Vat Brown R comprises the following steps: a. after acylation of 1,5-diaminoanthraquinone, 1-amino-5-benzamidoanthraquinone was prepared by acidic hydrolysis; b. 1-benzamido-4-bromoanthraquinone was obtained from 1-aminoanthraquinone by acylation and bromination; c. a condensate of Vat Brown R was obtained by condensation reaction of 1-amino-5-benzamidoanthraquinone and 1-benzamido-4-bromoanthraquinone; d. the original dye of Vat Brown R was obtained from the condensate of Vat Brown R by ring closing reaction and oxidation reaction. The method omits one oxidation step, economizes significant amount of oxidizing agent, and reduces significant amount of waste water, so it is very beneficial to environment protection; and the method also exhibited the advantages of highly increasing product yield and reducing the costs of raw materials to an extent of more than 30%.
Triazinyl dyes
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, (2008/06/13)
Vat dyestuffs of the formula EQU1 wherein R represents alkyl with 1 to 4 carbon atoms, R1 and R2 represent hydrogen or alkyl with 1 to 4 carbon atoms and each of A1 and A2 represents a vattable radical with 3 to 7 condensed rings are characterized by improved resistance to alkali and are suitable for dyeing and printing the most diverse materials, in particular fibers made from natural or regenerated cellulose.