138584

Sigma-Aldrich

3-Iodobenzoic acid

98%

Linear Formula:
IC6H4CO2H
CAS Number:
Molecular Weight:
248.02
Beilstein/REAXYS Number:
971088
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

mp

185-187 °C (lit.)

SMILES string

OC(=O)c1cccc(I)c1

InChI

1S/C7H5IO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,(H,9,10)

InChI key

KVBWBCRPWVKFQT-UHFFFAOYSA-N

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General description

3-Iodobenzoic acid is added as UV absorbing background electrolyte in separation of uncharged cyclodextrins and their derivatives by capillary electrophoresis.

Application

3-Iodobenzoic acid was used in solid phase synthesis of γ-turn mimetic library.

Packaging

10, 50 g in glass bottle

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

A γ-Turn Mimetic Library: Development and Production.
Kocis P, et al.
High-Throughput Synthesis: Principles and Practices, 65-65 (2010)
G Vaidyanathan et al.
Bioconjugate chemistry, 1(6), 387-393 (1990-11-01)
We have previously shown that use of N-succinimidyl 3-iodobenzoate (SIB) for radioiodination of monoclonal antibodies (MAbs) decreases the loss of radioiodine in vivo compared to MAbs labeled by using conventional methods. Herein, the synthesis of N-succinimidyl 2,4-dimethoxy-3-(trialkylstannyl)benzoates (alkyl = Me...
M Pumera et al.
Fresenius' journal of analytical chemistry, 369(7-8), 666-669 (2001-05-24)
A fast and simple capillary electrophoretic method suitable for the determination of native alpha-, beta-, gamma-cyclodextrins, their randomly substituted tert-butyl derivatives (average degree of substitution 3.8-4.4), heptakis (2,6-di-O-methyl)- and heptakis (2,3,6-tri-O-methyl)-beta-cyclodextrin was developed. Naphthyl-2-sulfonic acid (2-NSA), 3-iodobenzoic acid (3-IBA) and...
H Brasch
Archives internationales de pharmacodynamie et de therapie, 262(2), 242-249 (1983-04-01)
In guinea-pig Langendorff hearts, Na-salicylate (1.9, 3.8 and 7.6 mmol/l) concentration-dependently reduced the contractile force (--9.1, --51.0 and --75.1%, respectively) and the coronary resistance. The influence of the uncoupling agent 2.4-dinitrophenol (0.02 mmol/l) was comparable to that of the largest...
Pablo Wessig et al.
Molecules (Basel, Switzerland), 18(1), 1314-1324 (2013-01-23)
Various 1,6- and 1,8-naphthalenophanes were synthesized by using the Photo-Dehydro-Diels-Alder (PDDA) reaction of bis-ynones. These compounds are easily accessible from ω-(3-iodophenyl)carboxylic acids in three steps. The obtained naphthalenophanes are axially chiral and the activation barrier for the atropisomerization could be...

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