6337-00-4 Usage
Description
2-amino-3-bromoanthraquinone is a chemical compound that belongs to the anthraquinone dyes class. It is characterized by a bromine atom attached to the third carbon of the anthraquinone core and an amino group attached to the second carbon. This red-brown solid is known for its unique electronic properties and ability to absorb and emit light in the visible spectrum.
Uses
Used in Textile and Printing Industries:
2-amino-3-bromoanthraquinone is used as a dye and pigment for coloring fabrics and printed materials due to its vibrant red-brown color and stability.
Used in Ink, Plastics, and Coatings Manufacturing:
2-amino-3-bromoanthraquinone is used as a colorant in the production of inks, plastics, and coatings, providing a consistent and long-lasting color.
Used in Organic Electronic Devices:
2-amino-3-bromoanthraquinone is studied for its potential use in organic photovoltaics and light-emitting diodes due to its unique electronic properties and light absorption and emission capabilities in the visible spectrum.
Check Digit Verification of cas no
The CAS Registry Mumber 6337-00-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6337-00:
(6*6)+(5*3)+(4*3)+(3*7)+(2*0)+(1*0)=84
84 % 10 = 4
So 6337-00-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H8BrNO2/c15-11-5-9-10(6-12(11)16)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,16H2
6337-00-4Relevant articles and documents
Diazaheterocycle analogues of tetracene: Synthesis and properties of a naphtho-fused cinnoline and a naphtho-fused isoindazole
Young, Brian S.,Marshall, Jonathan L.,MacDonald, Ellen,Vonnegut, Chris L.,Haley, Michael M.
supporting information; experimental part, p. 5166 - 5168 (2012/06/04)
The synthesis and characterization of a diethynyl naphtho-fused cinnoline and isoindazole are described. The results show that both electron-accepting and electron-donating molecules can be prepared from a common intermediate.
