Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

367982

Sigma-Aldrich

2-Amino-5-fluorobenzoic acid

97%, for peptide synthesis

Synonym(s):

5-Fluoroanthranilic acid

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
H2NC6H3(F)CO2H
CAS Number:
446-08-2
Molecular Weight:
155.13
Beilstein:
2803664
EC Number:
207-159-7
MDL number:
MFCD00055566
UNSPSC Code:
12352106
PubChem Substance ID:
24862873
NACRES:
NA.22

product name

2-Amino-5-fluorobenzoic acid, 97%

Quality Level

100

Assay

97%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

mp

181-183 °C (lit.)

application(s)

peptide synthesis

SMILES string

Nc1ccc(F)cc1C(O)=O

InChI

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

InChI key

FPQMGQZTBWIHDN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service