A62205
2-Amino-3-methylbenzoic acid
99%
Synonym(s):
3-Methylanthranilic acid
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About This Item
Linear Formula:
H2NC6H3(CH3)CO2H
CAS Number:
Molecular Weight:
151.16
Beilstein:
2359694
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
powder, crystals or chunks
reaction suitability
reaction type: solution phase peptide synthesis
mp
174-177 °C (lit.)
application(s)
peptide synthesis
SMILES string
Cc1cccc(C(O)=O)c1N
InChI
1S/C8H9NO2/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4H,9H2,1H3,(H,10,11)
InChI key
WNAJXPYVTFYEST-UHFFFAOYSA-N
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Signal Word
Warning
Hazard 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
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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
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.
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