All Photos(1)
About This Item
Linear Formula:
BrC6H3(F)CO2H
CAS Number:
Molecular Weight:
219.01
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
form
solid
mp
172-176 °C (lit.)
SMILES string
OC(=O)c1ccc(F)cc1Br
InChI
1S/C7H4BrFO2/c8-6-3-4(9)1-2-5(6)7(10)11/h1-3H,(H,10,11)
InChI key
RRKPMLZRLKTDQV-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
Amination of 2-bromo-4-fluorobenzoic acid with aniline is reported to yield N-phenyl-4-fluoro-anthranilic acid.
Application
2-Bromo-4-fluorobenzoic acid may be used in the synthesis of:
- 3-fluoro-8-(methylthio)dibenzo[b,f]thiepin-10(11H)-one
- 2-fluoro-8-(methylthio)dibenzo[b,f]thiepin-10(11H)-one
- 2-((2-carboxy-5-fluorophenyl)amino)-3-methoxybenzoic acid
- 2-bromo-4-fluorobenzamide
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Lauren R Donaldson et al.
Organic & biomolecular chemistry, 9(7), 2233-2239 (2011-02-08)
A Heck cyclisation approach is described for the rapid synthesis of a library of natural product-like small molecules, based on the phenanthridine core. The synthesis of a range of substituted benzylamine building blocks and their incorporation into the library is
Neuroleptics with protracted action: 3-Fluoro derivatives of methiothepin and oxyprothepin and their 2-fluoro analogues.
Kopicova Z, et al.
Collection of Czechoslovak Chemical Communications, 40(11), 3519-3529 (1975)
Bernd Dörner et al.
Bioorganic & medicinal chemistry, 19(7), 2190-2198 (2011-03-23)
Aim of this study was to label the potent dual P-glycoprotein (Pgp) and breast cancer resistance protein (BCRP) inhibitor elacridar (1) with (18)F to provide a positron emission tomography (PET) radiotracer to visualize Pgp and BCRP. A series of new
Regioselective copper-catalyzed amination of bromobenzoic acids using aliphatic and aromatic amines.
Christian Wolf et al.
The Journal of organic chemistry, 71(8), 3270-3273 (2006-04-08)
A chemo- and regioselective copper-catalyzed cross-coupling procedure for amination of 2-bromobenzoic acids is described. The method eliminates the need for acid protection and produces N-aryl and N-alkyl anthranilic acid derivatives in up to 99% yield. N-(1-Pyrene)anthranilic acid has been employed
Fu-Xiang Wang et al.
Developmental cell, 54(6), 742-757 (2020-08-07)
Plant somatic embryogenesis refers to a phenomenon where embryos develop from somatic cells in the absence of fertilization. Previous studies have revealed that the phytohormone auxin plays a crucial role in somatic embryogenesis by inducing a cell totipotent state, although
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service