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About This Item
Linear Formula:
O2NC6H3(Br)CO2H
CAS Number:
Molecular Weight:
246.01
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
form
solid
mp
200-204 °C
functional group
bromo
carboxylic acid
nitro
SMILES string
OC(=O)c1ccc(c(Br)c1)[N+]([O-])=O
InChI
1S/C7H4BrNO4/c8-5-3-4(7(10)11)1-2-6(5)9(12)13/h1-3H,(H,10,11)
InChI key
KKPPNEJUUOQRLE-UHFFFAOYSA-N
Application
Substrate linked to a solid support via the carboxyl group which is used in a Bartoli synthesis of indoles.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
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
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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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