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138584

3-Iodobenzoic acid

98%

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About This Item

Linear Formula:
IC6H4CO2H
CAS Number:
618-51-9
Molecular Weight:
248.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848360
EC Number:
210-555-2
Beilstein/REAXYS Number:
971088
MDL number:
MFCD00002496
Assay:
98%
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Quality Level

200

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

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2609
BCCK6458
BCCD8176
BCCB1292
BCBW8707

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A γ-Turn Mimetic Library: Development and Production.
Kocis P, et al.
High-Throughput Synthesis: Principles and Practices, 65-65 (2010)
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
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
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Global Trade Item Number

SKUGTIN
138584-50G04061831828337
138584-10G04061838732378