943-14-6 Usage
Description
2-Bromo-5-nitrobenzoic acid is an organic compound characterized by the presence of a bromo and nitro functional group attached to a benzene ring, with a carboxylic acid group. It is a light beige to pale brown powder and is known for its chemical reactivity and potential applications in various fields.
Uses
Used in Chemical Synthesis:
2-Bromo-5-nitrobenzoic acid is used as a key intermediate in the synthesis of various organic compounds, including 2-bromo-5-nitrobenzophenone. Its unique structure allows for further functionalization and modification, making it a valuable building block in organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-bromo-5-nitrobenzoic acid may be utilized as a precursor for the development of new drugs or as a reagent in the synthesis of active pharmaceutical ingredients. Its chemical properties can be harnessed to create molecules with specific therapeutic effects.
Used in Research and Development:
2-Bromo-5-nitrobenzoic acid is also used in research and development settings, where it can be employed to study the effects of bromine and nitro substitutions on the chemical and physical properties of benzene derivatives. This knowledge can be applied to the design of new materials and compounds with tailored properties.
Used in Dye and Pigment Industry:
2-BROMO-5-NITROBENZOIC ACID may also find applications in the dye and pigment industry, where it can be used to produce colored compounds or as a starting material for the synthesis of complex dyes and pigments with specific color characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 943-14-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 943-14:
(5*9)+(4*4)+(3*3)+(2*1)+(1*4)=76
76 % 10 = 6
So 943-14-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrNO4/c8-6-2-1-4(9(12)13)3-5(6)7(10)11/h1-3H,(H,10,11)/p-1
943-14-6Relevant articles and documents
Donor-acceptor biaryl lactones: PH induced molecular switches with intramolecular charge transfer modulation
Carlson, Erik J.,Riel, Asia Marie S.,Dahl, Bart J.
supporting information, p. 6245 - 6249,5 (2012/12/11)
The physical properties of biaryl-containing compounds are known to be highly dependent on molecular geometry. We report the syntheses and fundamental spectroscopic study of two donor-acceptor biaryl lactone (6H-benzo[c]chromen-6- one) pH-driven switches.
Process for the production of nitro derivatives of aromatic compounds
-
, (2008/06/13)
Nitroderivates of aromatic compounds which are difficult to nitrate, can readily be obtained by nitration providing that the aromatic compound is treated with nitric acid or another nitrating agent in the presence of aliphatic or cycloaliphatic hydrocarbons monosubstituted or polysubstituted by halogen, the nitro group or an alkyl sulphonyl group, and the nitro derivative formed subsequently isolated.
