SMILES string
COc1ccc(N)c(c1)C(O)=O
InChI
1S/C8H9NO3/c1-12-5-2-3-7(9)6(4-5)8(10)11/h2-4H,9H2,1H3,(H,10,11)
InChI key
UMKSAURFQFUULT-UHFFFAOYSA-N
assay
97%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
148-152 °C
application(s)
peptide synthesis
Quality Level
Application
2-Amino-5-methoxybenzoic acid is a general reagent used in the synthesis of substituted isoquinolinonaphthyridines, quinazolinones, imidazobenzodiazepines, pyridoquinazolones and polycyclic hexahydrobenzo[c]acridines.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
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, Faceshields, Gloves
Biologically active heterocyclic hybrids based on quinazolinone, benzofuran and imidazolium moieties: synthesis, characterization, cytotoxic and antibacterial evaluation.
Asadi P, et al.
Chemistry and Biodiversity, 14(4), e1600411-e1600411 (2017)
Bismuth (III) Chloride Catalyzed Intramolecular Hetero-Diels?Alder Reaction: Access to cis-Fused Angular Hexahydrobenzo[c]acridines.
Sabitha G, et al.
Synthesis, 47(01), 124-128 (2015)
Optimization of substituted imidazobenzodiazepines as novel asthma treatments.
Jahan R, et al.
European Journal of Medicinal Chemistry, 126, 550-560 (2017)
Asymmetric synthesis of isoquinolinonaphthyridines catalyzed by a chiral Br?nsted acid.
Li J, et al.
Organic & Biomolecular Chemistry, 15(31), 6474-6477 (2017)
Condensation of anthranilic acids with pyridines to furnish pyridoquinazolones via pyridine dearomatization.
Yang Y, et al.
Chemical Communications (Cambridge, England), 52(87), 12869-12872 (2016)
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