Skip to Content
Merck
All Photos(3)

Documents

Safety Information

412244

Sigma-Aldrich

2-Fluorobenzoic acid

97%

Synonym(s):

o-Fluorobenzoic acid

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
FC6H4CO2H
CAS Number:
445-29-4
Molecular Weight:
140.11
Beilstein:
971265
EC Number:
207-158-1
MDL number:
MFCD00002405
UNSPSC Code:
12352100
PubChem Substance ID:
24865797
NACRES:
NA.22

Assay

97%

mp

122-125 °C (lit.)

SMILES string

OC(=O)c1ccccc1F

InChI

1S/C7H5FO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)

InChI key

NSTREUWFTAOOKS-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

2-Fluorobenzoic acid may be employed in the preparation of zaragozic acid A analogs.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

412244-BULK:
412244-5KG:
412244-VAR:
412244-100G:
412244-25G:

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

Microbial degradation of synthetic organochlorine compounds.
K Motosugi et al.
Experientia, 39(11), 1214-1220 (1983-11-15)
J Toretsky et al.
Nuclear medicine and biology, 31(6), 747-752 (2004-07-13)
The clinical response to antitumor therapy is measured using imaging, such as CT or MRI, 6-12 weeks following chemotherapy treatment. The images at that time reflect both tumor cell death and new growth. Therefore, the amount of tumor cell death
S Y Lee et al.
Nuclear medicine and biology, 28(4), 391-395 (2001-06-08)
In vitro metabolism of acetylcholinesterase inhibitors containing 3-[(18)F]fluoromethylbenzyl- ([(18)F]1) and 4-[(18)F]fluorobenzyl-piperidine moieties ([(18)F]2) was studied and compared with the in vivo metabolism. Defluorination of the [(18)F]1 mainly occurred to generate [(18)F]fluoride ion both in vitro and in vivo. In contrast
O Drzyzga et al.
FEMS microbiology letters, 116(2), 215-219 (1994-02-15)
A mesophilic, dehalogenating, sulfate-reducing diculture was isolated from an anaerobic lake sediment. One strain of the diculture is proposed to be an endospore-forming Desulfotomaculum species, the second strain was a vibrioid, motile and non-sporeforming species which is tentatively assigned to
T S Chen et al.
The Journal of antibiotics, 47(11), 1290-1294 (1994-11-01)
Zaragozic acid A analogues are produced by an unidentified sterile fungus when it is exogenously supplied with 2-thiophenecarboxylic acid, 3-thiophenecarboxylic acid, 2-furoic acid, 2-fluorobenzoic acid, 3-fluorobenzoic acid, or 4-fluorobenzoic acid. The analogues carry 2-thiophenyl, 3-thiophenyl, 2-furyl, o-fluorophenyl, m-fluorophenyl, or p-fluorophenyl
View All Related Papers

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