56287-72-0 Usage
Uses
Used in Organic Synthesis:
BENZAMIDE, 2-[(2-FLUOROACETYL)AMINO]-N-(2-METHYLPHENYL)-5-NITROis used as an intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows it to be a key component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, BENZAMIDE, 2-[(2-FLUOROACETYL)AMINO]-N-(2-METHYLPHENYL)-5-NITROis used as a building block for the development of new drugs. Its versatile structure enables the creation of potential therapeutic agents that can target a wide range of diseases and conditions.
Used in Agrochemical Industry:
BENZAMIDE, 2-[(2-FLUOROACETYL)AMINO]-N-(2-METHYLPHENYL)-5-NITROis also used in the agrochemical industry as a precursor for the synthesis of pesticides and other crop protection agents. Its chemical properties make it suitable for the development of effective and environmentally friendly agrochemicals.
Used in Specialty Chemicals:
In the specialty chemicals sector, BENZAMIDE, 2-[(2-FLUOROACETYL)AMINO]-N-(2-METHYLPHENYL)-5-NITROis employed as a key component in the production of various specialty chemicals, such as dyes, pigments, and coatings. Its unique properties contribute to the development of innovative and high-performance products in this industry.
Check Digit Verification of cas no
The CAS Registry Mumber 56287-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,8 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56287-72:
(7*5)+(6*6)+(5*2)+(4*8)+(3*7)+(2*7)+(1*2)=150
150 % 10 = 0
So 56287-72-0 is a valid CAS Registry Number.
56287-72-0Relevant articles and documents
2-Fluoromethyl-3-o-tolyl-6-amino-4(3H)-quinazolinone
-
, (2008/06/13)
N-(2-amino-5-nitrobenzoyl)-o-toluidine is condensed with fluoroacetic acid or a functional derivative thereof. N-(2-fluoroacetamido-5-nitrobenzoyl)-o-toluidine obtained by said condensation reaction is dehydrated to produce 2-fluoromethyl-3-(o-tolyl)-6-nitro-4(3H)-quniazolinone, which is then subjected to reduction reaction. 2-fluoromethyl-3-(o-tolyl)-6-amino-4(3H)-quinazolinone thus obtained and a pharmaceutically acceptable acid addition salt thereof are useful as central muscle relaxants, minor tranquilizers, anti-convulsants, analgesics and/or anti-inflammatory agents.