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3-Iodobenzoic acid

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CAS:618-51-9
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  • 3-Iodobenzoic acid
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  • CAS:618-51-9
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  • CAS:618-51-9
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  • 2022-02-22
  • CAS:618-51-9
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3-Iodobenzoic acid Basic information
Product Name:3-Iodobenzoic acid
Synonyms:3-Iodobenzoic acid,95%;3-IODOBENZOIC ACID;Acid between the iodine;3-Carboxyiodobenzene;3-Iodobenzoic acid, 98% 10GR;Iodobenzoic aci;Pemetrexed disodium Impurity 10;m-Carboxyiodobenzene
CAS:618-51-9
MF:C7H5IO2
MW:248.02
EINECS:210-555-2
Product Categories:Pharmaceutical Intermediates;Aromatics;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Carboxylic Acids;Phenyls & Phenyl-Het;Benzoic acid;API intermediates;C7;Carbonyl Compounds;Carboxylic Acids;Phenyls & Phenyl-Het;Acids & Esters;Iodine Compounds;bc0001
Mol File:618-51-9.mol
3-Iodobenzoic acid Structure
3-Iodobenzoic acid Chemical Properties
Melting point 185-187 °C(lit.)
Boiling point 337.2±25.0 °C(Predicted)
density 2.2170 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform, Methanol
pka3.8(at 25℃)
form Powder
color White to beige
Water Solubility Soluble in Chloroform and Methanol. Insoluble in water.
Sensitive Light Sensitive
BRN 971088
InChIInChI=1S/C7H5IO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,(H,9,10)
InChIKeyKVBWBCRPWVKFQT-UHFFFAOYSA-N
SMILESC(O)(=O)C1=CC=CC(I)=C1
CAS DataBase Reference618-51-9(CAS DataBase Reference)
NIST Chemistry ReferenceBenzoic acid, 3-iodo-(618-51-9)
EPA Substance Registry SystemBenzoic acid, 3-iodo- (618-51-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-37/39-26
WGK Germany 3
Hazard Note Irritant
TSCA TSCA listed
HazardClass IRRITANT, LIGHT SENSITIVE
HS Code 29163990
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
3-Iodobenzoic acid English
SigmaAldrich English
ACROS English
ALFA English
3-Iodobenzoic acid Usage And Synthesis
Description3-Iodobenzoic acid is added as UV absorbing background electrolyte in separation of uncharged cyclodextrins and their derivatives by capillary electrophoresis.3-Iodobenzoic acid was used in solid phase synthesis of γ-turn mimetic library.
Chemical Propertieswhite to beige powder
Usessuzuki reaction
Uses3-Iodobenzoic acid is used in solid phase synthesis of γ-turn mimetic library. It is used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff.
Uses3-Iodobenzoic acid was used in solid phase synthesis of γ-turn mimetic library.
DefinitionChEBI: 3-iodobenzoic acid is an iodobenzoic acid with a single iodo substituent placed at the 3-position.
General Description3-Iodobenzoic acid is added as UV absorbing background electrolyte in separation of uncharged cyclodextrins and their derivatives by capillary electrophoresis.
Synthesis
3-Carboxyphenylboronic acid

25487-66-5

3-Iodobenzoic acid

618-51-9

The general procedure for the synthesis of 3-iodobenzoic acid from 3-carboxyphenylboronic acid was as follows: arylboronic acid 1 (0.5 mmol) and K2CO3 (1 mmol, 138.0 mg) were added to a 20 mL Schlenk tube fitted with a non-magnetic stir bar. The Schlenk tube was evacuated twice and backfilled with N2. MeCN (2 mL) and I2 (0.75 mmol, 191 mg) were added to the tube at room temperature. The Schlenk tube was sealed and placed in a preheated oil bath at 80 °C for 8-12 h under a stream of N2 gas. After completion of the reaction, the resulting solution was cooled to room temperature. H2O (10 mL) was added, and for the product 3-iodobenzoic acid, 1 M HCl was added to the aqueous solution until the pH reached 2 prior to extraction.The aqueous layer was extracted with EtOAc (3 x 5 mL). The organic phases were combined, dried with anhydrous Na2SO4, filtered and concentrated by rotary evaporation. Finally, the residue was purified by silica gel column chromatography to obtain the target product 3-iodobenzoic acid.

Purification MethodsCrystallise the acid repeatedly from water and EtOH. Sublime it under vacuum at 100o. [Beilstein 9 IV 1033.]
References[1] Synlett, 2014, vol. 25, # 7, p. 995 - 1000
[2] Chemistry - A European Journal, 2011, vol. 17, # 20, p. 5652 - 5660
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