59333-62-9 Usage
Description
2-Octylisoindoline-1,3-dione is a synthetic yellow pigment with the molecular formula C18H21NO2. It is known for its high heat stability, lightfastness, and weather resistance, making it a popular choice for various applications.
Uses
Used in Inks, Coatings, and Plastics Industry:
2-Octylisoindoline-1,3-dione is used as a colorant for its high heat stability, lightfastness, and weather resistance, making it suitable for outdoor applications.
Used in Textile Industry:
2-Octylisoindoline-1,3-dione is used as a coloring agent in the dyeing of polyester fibers due to its high tinting strength and excellent dispersion properties.
It is important to handle 2-Octylisoindoline-1,3-dione with care due to its potential for skin and eye irritation.
Check Digit Verification of cas no
The CAS Registry Mumber 59333-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,3 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59333-62:
(7*5)+(6*9)+(5*3)+(4*3)+(3*3)+(2*6)+(1*2)=139
139 % 10 = 9
So 59333-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H21NO2/c1-2-3-4-5-6-9-12-17-15(18)13-10-7-8-11-14(13)16(17)19/h7-8,10-11H,2-6,9,12H2,1H3
59333-62-9Relevant articles and documents
Direct Synthesis of Cyclic Imides from Carboxylic Anhydrides and Amines by Nb2O5 as a Water-Tolerant Lewis Acid Catalyst
Ali, Md. A.,Moromi, Sondomoyee K.,Touchy, Abeda S.,Shimizu, Ken-Ichi
, p. 891 - 894 (2016/03/15)
In the 20 types of heterogeneous and homogenous catalysts screened, Nb2O5 showed the highest activity for the synthesis of N-phenylsuccinimide by dehydrative condensation of succinic anhydride and aniline. Nb2O5 was used in the direct imidation of a wide range of carboxylic anhydrides with NH3 or amines with various functional groups and could be reused. Kinetic studies showed that the Lewis acid Nb2O5 catalyst was more water tolerant than both the Lewis acidic oxide TiO2 and the homogeneous Lewis acid ZrCl4, which resulted in higher yields of imides through the use of Nb2O5. Int-imidation tactics: A general method for the direct synthesis of cyclic imides from cyclic anhydrides with amines (or ammonia) under solvent-free conditions is reported. Kinetic studies indicate that the Lewis acid sites of Nb2O5 are highly water tolerant, which results in high catalytic activity for imidation even in the presence of water formed during the reaction. The catalyst can be recovered and reused four times without a marked decrease in yield.