81-44-7

Basic information

• Product Name: 1-BENZOYLAMINO-4-BROMOANTHRAQUINONE
• Synonyms: 1-BENZOYLAMINO-4-BROMOANTHRAQUINONE;N-(4-bromo-9,10-dihydro-9,10-dioxo-1-anthryl)benzamide;N-(4-bromo-9,10-diketo-1-anthryl)benzamide;N-(4-bromo-9,10-dioxo-anthracen-1-yl)benzamide;N-(4-bromo-9,10-dioxoanthracen-1-yl)benzamide
• CAS NO: 81-44-7
• Molecular Formula: C₂₁H₁₂BrNO₃
• Molecular Weight: 406.23
• EINECS: 201-349-3
• Mol File: 81-44-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 518.4°C at 760 mmHg
• Flash Point: 267.3°C
• Appearance: /
• Density: 1.598g/cm³
• Vapor Pressure: 7.53E-11mmHg at 25°C
• Refractive Index: 1.725
• CAS DataBase Reference: 1-BENZOYLAMINO-4-BROMOANTHRAQUINONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BENZOYLAMINO-4-BROMOANTHRAQUINONE(81-44-7)
• EPA Substance Registry System: 1-BENZOYLAMINO-4-BROMOANTHRAQUINONE(81-44-7)

Safety Data

• Hazardous Substances Data: 81-44-7(Hazardous Substances Data)

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.

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)

Upstream product

• 3571-23-1 N-(9,10-dioxo-9,10-dihydro-[1]anthryl)-benzamide 
• 82-45-1 1-amino-9,10-anthracenedione 
• 98-88-4 benzoyl chloride 
• 7726-95-6 bromine 
• 7705-08-0 iron(III) chloride 
• 98-95-3 nitrobenzene 
• 81-62-9 1-amino-4-bromo-9,10-anthracenedione 

Downstream Products

• 6409-75-2 1-benzamido-4-methoxy-9,10-anthraquinone 
• 129586-65-8 4-bromo-N-benzoyl-1-methylaminoanthraquinone 
• 128-89-2 4,5'-bis-benzoylamino-1,1'-imino-di-anthraquinone 

Relevant articles and documents

PREPARATION METHOD OF ORIGINAL DYE OF VAT BROWN R

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%.