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About This Item
Linear Formula:
H2NC6H3(CH3)CO2H
CAS Number:
Molecular Weight:
151.16
UNSPSC Code:
12352200
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-505-2
Beilstein/REAXYS Number:
2359694
MDL number:
Product Name
2-Amino-3-methylbenzoic acid, 99%
InChI key
WNAJXPYVTFYEST-UHFFFAOYSA-N
InChI
1S/C8H9NO2/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4H,9H2,1H3,(H,10,11)
SMILES string
Cc1cccc(C(O)=O)c1N
assay
99%
form
powder, crystals or chunks
reaction suitability
reaction type: solution phase peptide synthesis
mp
174-177 °C (lit.)
application(s)
peptide synthesis
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R C Kammerer et al.
Xenobiotica; the fate of foreign compounds in biological systems, 16(7), 681-690 (1986-07-01)
Metabolism of lidocaine in rabbit liver 9000 g supernatant fraction was examined. A capillary g.l.c. assay was developed to separate seven known metabolites of lidocaine, and all seven metabolites were identified in extracts of incubations of lidocaine with rabbit-liver fractions.
Derek Maclean et al.
Journal of combinatorial chemistry, 6(2), 196-206 (2004-03-09)
The design, synthesis, characterization, and screening of a large, encoded thiazolidinone library are described. Three sets of 35 building blocks were combined by encoded split-pool synthesis to give a library containing more than 42 000 members. Building block selection was
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