400-67-9 Usage
Description
2-AMINO-3-CHLORO-5-NITROBENZOTRIFLUORIDE is an organic compound characterized by its unique molecular structure, which features a benzene ring with a trifluoromethyl group, a chloro substituent, a nitro group, and an amino group. 2-AMINO-3-CHLORO-5-NITROBENZOTRIFLUORIDE is known for its chemical reactivity and potential applications in various industries due to its functional groups.
Uses
Used in Chemical Synthesis:
2-AMINO-3-CHLORO-5-NITROBENZOTRIFLUORIDE is used as a key intermediate in the synthesis of various organic compounds, particularly in the production of monoazo dyes. Its presence in the molecular structure allows for the formation of a wide range of dyes with different colors and properties, making it a valuable component in the chemical industry.
Used in Dye Manufacturing:
In the dye manufacturing industry, 2-AMINO-3-CHLORO-5-NITROBENZOTRIFLUORIDE is used as a starting material for the preparation of monoazo dyes. These dyes are widely used in various applications, including textiles, plastics, and printing inks, due to their colorfastness and versatility. 2-AMINO-3-CHLORO-5-NITROBENZOTRIFLUORIDE's unique structure enables the creation of dyes with specific color characteristics, catering to the diverse needs of the dye industry.
Used in Pharmaceutical Research:
2-AMINO-3-CHLORO-5-NITROBENZOTRIFLUORIDE may also find applications in the pharmaceutical industry, particularly in the development of new drugs. Its chemical structure can be modified to create potential drug candidates with various therapeutic properties. Researchers can explore its potential in the development of novel compounds for treating various diseases and conditions.
Used in Research and Development:
Due to its unique chemical properties, 2-AMINO-3-CHLORO-5-NITROBENZOTRIFLUORIDE can be utilized in research and development laboratories for various purposes. It can serve as a building block for the synthesis of new compounds, a reagent in chemical reactions, or a model compound for studying the effects of its functional groups on the overall properties of the molecule.
Check Digit Verification of cas no
The CAS Registry Mumber 400-67-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 400-67:
(5*4)+(4*0)+(3*0)+(2*6)+(1*7)=39
39 % 10 = 9
So 400-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClF3N2O2/c8-5-2-3(13(14)15)1-4(6(5)12)7(9,10)11/h1-2H,12H2
400-67-9Relevant articles and documents
SUBSTITUTED ANILINE DERIVATIVES
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Page/Page column 60-61, (2008/06/13)
The present invention relates to aniline derivatives of the general formula (I) or salts thereof and their use, related to their KCNQ potassium ion channel opening activity.