138584
3-Iodobenzoic acid
98%
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About This Item
Fórmula lineal:
IC6H4CO2H
Número de CAS:
Peso molecular:
248.02
Beilstein/REAXYS Number:
971088
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
mp
185-187 °C (lit.)
functional group
carboxylic acid
iodo
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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Categorías relacionadas
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.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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A γ-Turn Mimetic Library: Development and Production.
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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
Negative inotropic effects of Na-salicylate and three congeners on the guinea-pig Langendorff heart.
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.
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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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