1007-16-5 Usage
Description
3-Bromo-4-fluorobenzoic acid is an organic compound that belongs to the class of benzoic acids. It is characterized by the presence of a bromine atom at the 3rd position and a fluorine atom at the 4th position on the benzene ring. This white to light yellow crystal powder exhibits unique chemical properties that make it suitable for various applications in different industries.
Uses
Used in Chemical Synthesis:
3-Bromo-4-fluorobenzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structural features allow for further functionalization and modification, making it a versatile building block in the development of new molecules with specific biological activities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Bromo-4-fluorobenzoic acid is used as a starting material for the synthesis of drugs with potential therapeutic applications. Its chemical properties enable the creation of novel drug candidates that can target specific biological pathways, offering new treatment options for various diseases.
Used in Agrochemical Industry:
3-Bromo-4-fluorobenzoic acid is also utilized in the agrochemical industry for the development of new pesticides and other crop protection agents. Its structural diversity allows for the design of compounds with improved efficacy and selectivity, contributing to more sustainable and environmentally friendly agricultural practices.
Used in Research and Development:
In the field of research and development, 3-Bromo-4-fluorobenzoic acid serves as an important compound for studying various chemical reactions and mechanisms. Its unique properties make it a valuable tool for understanding the reactivity of different functional groups and for developing new synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 1007-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1007-16:
(6*1)+(5*0)+(4*0)+(3*7)+(2*1)+(1*6)=35
35 % 10 = 5
So 1007-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrFO2/c8-5-3-4(7(10)11)1-2-6(5)9/h1-3H,(H,10,11)/p-1
1007-16-5Relevant articles and documents
An efficient one pot method for synthesis of carboxylic acids from nitriles using recyclable ionic liquid [bmim]HSO4 Dedicated to my mentor Professor (Mrs.) Krishna Misra on her 76th birthday
Kumar, Satyanand,Dixit, Sandeep Kumar,Awasthi, Satish Kumar
, p. 3802 - 3804 (2014)
Environmentally benign ionic liquid [bmim]HSO4 was found suitable for conversion of nitriles into carboxylic acids under mild conditions with excellent purity.
Halogens halt aromatic group migration in Baeyer-Villiger oxidation
Adejare, Adeboye,Shen, Jun,Ogunbadeniyi, Alaba M.
, p. 107 - 109 (2000)
Oxidation of a dihalogenated benzaldehyde under Baeyer-Villiger conditions led to the aromatic carboxylic acid as opposed to the desired phenol. Fluorine was located at the para-position of the benzaldehyde, halting migration of the aryl group and thus resulting in the carboxylic acid product.
GLUCOSE-SENSITIVE ALBUMIN-BINDING DERIVATIVES
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Page/Page column 67, (2019/05/30)
This invention relates to glucose-sensitive albumin-binding diboron conjugates. More particularly the invention provides novel diboron compounds, and in particular diboronate or diboroxole compounds, useful as intermediate compounds for the synthesis of diboron conjugates. The diboron compounds are characterized by formula (I), which is: R1-X-R2, and wherein "X" is a mono- to multiatomic linker and where R1 and R2, which may be identical or different, each represents a group of Formula (lla) or (IIb) Also described are diboron conjugates represented by the general Formula (I'), which is: R1'-X'-R2', in which either the moeities R1' or R2' or X' carry a drug that is covalently attached to the diboron compound.
A Metal-Free Approach to Carboxylic Acids by Oxidation of Alkyl, Aryl, or Heteroaryl Alkyl Ketones or Arylalkynes
Aravinda Kumar,Venkateswarlu, Vunnam,Vishwakarma, Ram A.,Sawant, Sanghapal D.
, p. 3161 - 3168 (2015/10/19)
The metal-free oxidation of dialkyl, alkyl aryl, or alkyl heteroaryl ketones or arylalkynes to the corresponding carboxylic acids is achieved using an oxidative mixture of Oxone and trifluoroacetic acid. This green method is a simple and mild protocol to obtain carboxylic derivatives in excellent yields.
