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
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
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)
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
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 420291-100GM | 04055977210859 |
| 420291-1GM | 04055977210835 |
| 420291-1KG | 04055977210842 |
| 420291-5GM | 07790788050108 |
| 420322-10GM | 07790788055622 |
| 420322-1KG | 04055977210569 |
| 420322-500GM | 07790788050153 |
| I6758-1G | 04061835367078 |
| I6758-10G | 04061835367061 |
| I6758-5G | 04061835367085 |
| I5502-1G | 04061838446190 |
| I1284-5ML | 04061833847640 |
| PHG0010-5G | 04061832608594 |
| PHG0010-1000G | 04061826004838 |
| 5815-25GM | 04055977242416 |
| 10724815001 | 04061838674692 |
| 11411446001 | 04061838701701 |
| 15-2461-3-5G-J | 04061832684895 |
| 420290-5GM | 04055977210828 |
| 420322-100GM | 07790788050146 |
| 420322-1GM | 04055977210552 |