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About This Item
Linear Formula:
H2NC6H3(OCH3)CO2H
CAS Number:
Molecular Weight:
167.16
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
reaction suitability
reaction type: solution phase peptide synthesis
mp
186-188 °C (lit.)
application(s)
peptide synthesis
SMILES string
COc1cc(ccc1N)C(O)=O
InChI
1S/C8H9NO3/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4H,9H2,1H3,(H,10,11)
InChI key
JNFGLYJROFAOQP-UHFFFAOYSA-N
Application
Key building block for the efficient synthesis of carbazole alkaloids mukonine and mukonidine via oxidative annulation.
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
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Tetrahedron, 59, 5317-5317 (2003)
Domenico Pirone et al.
Polymers, 12(5) (2020-05-06)
A molecular design approach was used to create asymmetrical visible light-triggered azo-derivatives that can be good candidates for polymer functionalization. The specific electron-donor substituted molecules were characterized and studied by means of NMR analyses and UV-visible spectroscopy, comparing the results
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