96155-99-6 Usage
Uses
Used in Pharmaceutical Industry:
4,5-Dimethyl-3-(1-methylethyl)benzenamine is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications. Its role in this industry is crucial for creating active pharmaceutical ingredients and enhancing the therapeutic properties of medications.
Used in Agrochemical Industry:
In the agrochemical sector, 4,5-Dimethyl-3-(1-methylethyl)benzenamine serves as a key intermediate in the production of agrochemicals, which are essential for crop protection and increasing agricultural productivity. Its involvement in this industry aids in the development of effective pesticides and other agricultural chemicals.
Used in Dye and Pigment Industry:
4,5-Dimethyl-3-(1-methylethyl)benzenamine is utilized as an intermediate in the manufacturing process of dyes and pigments, which are vital for coloring textiles, plastics, and various other materials. Its application in this industry ensures the creation of a wide range of colorants with diverse properties and uses.
Used in Industrial Chemical Production:
4,5-Dimethyl-3-(1-methylethyl)benzenamine also finds application in the broader field of industrial chemical production, where it acts as a versatile intermediate for synthesizing a variety of chemical products. Its presence in this industry highlights its adaptability and importance in multiple chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 96155-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,5 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96155-99:
(7*9)+(6*6)+(5*1)+(4*5)+(3*5)+(2*9)+(1*9)=166
166 % 10 = 6
So 96155-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N/c1-7(2)11-6-10(12)5-8(3)9(11)4/h5-7H,12H2,1-4H3
96155-99-6Relevant academic research and scientific papers
Conformational Analysis of Trigonal and Planar Rotors attached to Δ4-Azoline-2-thiones. The Effect of Ring Geometry
Djafri, Ayada,Roussel, Christian,Sandstroem, Jan
, p. 273 - 278 (2007/10/02)
The barriers to rotation of isopropyl and aryl groups (unsubstituted in the ortho positions) in position 3 in 4,5-dimethyl-oxazoline-2-thiones, -imidazoline-2-thiones, and -thiazoline-2-thiones have been studied by temperature-dependent 1H n.m.r. spectra.
