659304
3-Bromo-4-nitrobenzoic acid
97%
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About This Item
Linear Formula:
O2NC6H3(Br)CO2H
CAS Number:
Molecular Weight:
246.01
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
InChI
1S/C7H4BrNO4/c8-5-3-4(7(10)11)1-2-6(5)9(12)13/h1-3H,(H,10,11)
SMILES string
OC(=O)c1ccc(c(Br)c1)[N+]([O-])=O
InChI key
KKPPNEJUUOQRLE-UHFFFAOYSA-N
assay
97%
form
solid
mp
200-204 °C
functional group
bromo, carboxylic acid, nitro
Application
Substrate linked to a solid support via the carboxyl group which is used in a Bartoli synthesis of indoles.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Kerstin Knepper et al.
Organic letters, 5(16), 2829-2832 (2003-08-02)
[reaction: see text] Bartoli indole synthesis has been performed for the first time on solid supports. Starting from Merrifield resin, immobilization of five nitro benzoic acids was performed. Addition of four different alkenyl Grignard reagents and basic cleavage leads to
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