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367982

2-Amino-5-fluorobenzoic acid

97%, for peptide synthesis

Synonym(s):

5-Fluoroanthranilic acid

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About This Item

Linear Formula:
H2NC6H3(F)CO2H
CAS Number:
Molecular Weight:
155.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
207-159-7
MDL number:
Beilstein/REAXYS Number:
2803664

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Product Name

2-Amino-5-fluorobenzoic acid, 97%

InChI key

FPQMGQZTBWIHDN-UHFFFAOYSA-N

InChI

1S/C7H6FNO2/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3H,9H2,(H,10,11)

SMILES string

Nc1ccc(F)cc1C(O)=O

assay

97%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

Quality Level

application(s)

peptide synthesis

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1 of 4

This Item
278998340871123188
form

solid

form

solid

form

solid

form

solid

assay

97%

assay

98%

assay

95%

assay

97%

mp

181-183 °C (lit.)

mp

247 °C (dec.) (lit.)

mp

206 °C (dec.) (lit.)

mp

158-161 °C (lit.)

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

200

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

reaction type: solution phase peptide synthesis

reaction suitability

reaction type: solution phase peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

application(s)

peptide synthesis

Application

Used in the synthesis of styrylquinazolinones which are potential anticancer agents.[1]

pictograms

Exclamation mark

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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J B Jiang et al.
Journal of medicinal chemistry, 33(6), 1721-1728 (1990-06-01)
A novel series of 2-styrylquinazolin-4(3H-ones which inhibited tubulin polymerization and the growth of L1210 murine leukemia cells was discovered. Extensive structure-activity relationship studies suggest that the entire quinazolinone structure was required, but activity was further enhanced by halide or small
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
Marcela Briones-Martin-del-Campo et al.
Microbiology (Reading, England), 161(Pt 2), 300-310 (2014-12-07)
The fungal pathogen Candida glabrata has a well-defined oxidative stress response, is extremely resistant to oxidative stress and can survive inside phagocytic cells. In order to further our understanding of the oxidative stress response in C. glabrata, we characterized the

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