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A62205

Sigma-Aldrich

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:
4389-45-1
Molecular Weight:
151.16
Beilstein/REAXYS Number:
2359694
EC Number:
224-505-2
MDL number:
MFCD00007745
UNSPSC Code:
12352200
PubChem Substance ID:
24891068
NACRES:
NA.22

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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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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