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Merck

419443

2-Amino-5-methylbenzoic acid

99%

Synonym(s):

5-Methylanthranilic acid

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About This Item

Linear Formula:
H2NC6H3(CH3)CO2H
CAS Number:
2941-78-8
Molecular Weight:
151.16
NACRES:
NA.22
PubChem Substance ID:
24866108
eCl@ss:
32160406
UNSPSC Code:
12352106
EC Number:
220-932-3
MDL number:
MFCD00007909
Beilstein/REAXYS Number:
1101527

Key Documents

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InChI key

NBUUUJWWOARGNW-UHFFFAOYSA-N

InChI

1S/C8H9NO2/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4H,9H2,1H3,(H,10,11)

SMILES string

Cc1ccc(N)c(c1)C(O)=O

assay

99%

reaction suitability

reaction type: solution phase peptide synthesis

mp

175 °C (dec.) (lit.)

application(s)

peptide synthesis

Quality Level

100

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General description

2-Amino-5-methylbenzoic acid also known as 5-methylanthranilic acid, is often used in the solution-phase peptide synthesis.

Application

2-Amino-5-methylbenzoic acid can be used to synthesize quinazolinedione.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000467165
0000467165
0000452654
0000452654
0000435671

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Synthesis and evaluation of quinazolines as inhibitors of the bacterial cell division protein FtsZ
GM Nepomuceno
ACS Medicinal Chemistry Letters, 6, 308-312 (2015)
João Daniel Santos Fernandes et al.
PloS one, 10(7), e0132369-e0132369 (2015-07-15)
Metabolic diversity is an important factor during microbial adaptation to different environments. Among metabolic processes, amino acid biosynthesis has been demonstrated to be relevant for survival for many microbial pathogens, whereas the association between pathogenesis and amino acid uptake and

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