419443
2-アミノ-5-メチル安息香酸
99%
別名:
5-メチルアントラニル酸
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この商品について
化学式:
H2NC6H3(CH3)CO2H
CAS番号:
分子量:
151.16
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352106
EC Number:
220-932-3
MDL number:
Beilstein/REAXYS Number:
1101527
Quality Level
assay
99%
reaction suitability
reaction type: solution phase peptide synthesis
mp
175 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
Cc1ccc(N)c(c1)C(O)=O
InChI
1S/C8H9NO2/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4H,9H2,1H3,(H,10,11)
InChI key
NBUUUJWWOARGNW-UHFFFAOYSA-N
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
保管分類
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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