63133-82-4 Usage
Description
2-Chloro-4,6-dimethylaniline is an aromatic amine that serves as an organic building block in chemical synthesis. It is characterized by its distinct chemical properties, including a boiling point, freezing point, density, and refractive index.
Uses
Used in Chemical Synthesis Industry:
2-Chloro-4,6-dimethylaniline is used as a key intermediate in the synthesis of various organic compounds for [application reason]. Its unique structure and reactivity make it a valuable component in the creation of a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Chloro-4,6-dimethylaniline is utilized as a building block for the development of new drugs, specifically for [application reason]. Its presence in the molecular structure can contribute to the desired pharmacological properties of the final drug product.
Used in Dye and Pigment Industry:
2-Chloro-4,6-dimethylaniline is employed as a precursor in the production of dyes and pigments, particularly for [application reason]. Its aromatic nature and reactivity allow for the creation of a diverse palette of colors and shades.
Used in Agrochemical Industry:
Within the agrochemical field, 2-Chloro-4,6-dimethylaniline is used as a starting material for the synthesis of various agrochemicals, such as herbicides, pesticides, and fungicides, for [application reason]. Its role in these products is crucial for enhancing crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 63133-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,3 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63133-82:
(7*6)+(6*3)+(5*1)+(4*3)+(3*3)+(2*8)+(1*2)=104
104 % 10 = 4
So 63133-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClN/c1-5-3-6(2)8(10)7(9)4-5/h3-4H,10H2,1-2H3
63133-82-4Relevant articles and documents
N-phenyl-N'-pyridinylureas as anticonvulsant agents
Pavia,Lobbestael,Taylor,Hershenson,Miskell
, p. 854 - 861 (2007/10/02)
A series of N-phenyl-N'-pyridinylureas was examined for anticonvulsant activity. Extensive structure/activity investigations revealed optimal activity in the N-(2,6-disubstituted-phenyl)-N'-(4-pyridinyl)urea series, with 37 exhibiting the best overall anticonvulsant profile. Compound 37 was effective against seizures induced by maximal electroshock but did not protect mice from clonic seizures produced by the convulsant pentylenetetrazol. The overall pharmacological profile suggests that 37 would be of therapeutic use in the treatment of generalized tonic-clonic and partial seizures. Compound 37 was selected for Phase 1 clinical trials.
