419443
2-氨基-5-甲基苯甲酸
99%
别名:
5-甲基邻氨基苯甲酸
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关于此项目
线性分子式:
H2NC6H3(CH3)CO2H
化学文摘社编号:
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
产品名称
2-氨基-5-甲基苯甲酸, 99%
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
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Application
2-Amino-5-methylbenzoic acid can be used to synthesize quinazolinedione.
General description
2-Amino-5-methylbenzoic acid also known as 5-methylanthranilic acid, is often used in the solution-phase peptide synthesis.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
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
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