CAS 58313-23-8

3-Iodobenzoic acid ethyl ester

Description:

3-Iodobenzoic acid ethyl ester is an organic compound characterized by its structure, which includes a benzoic acid moiety substituted with an iodine atom at the meta position and an ethyl ester functional group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is known for its moderate solubility in organic solvents such as ethanol and dichloromethane, while being less soluble in water due to the hydrophobic nature of the aromatic ring and the ethyl ester group. The presence of the iodine atom imparts unique reactivity, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions in organic synthesis. Additionally, 3-iodobenzoic acid ethyl ester can serve as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety precautions should be observed when handling this compound, as iodine-containing compounds can be hazardous. Proper storage conditions are also essential to maintain its stability and prevent degradation.

Formula: C₉H₉IO₂

InChI: InChI=1/C9H9IO2/c1-2-12-9(11)7-4-3-5-8(10)6-7/h3-6H,2H2,1H3

SMILES: CCOC(=O)c1cccc(c1)I

Synonyms:

• Ethyl 3-iodobenzoate
• Ethyl iodobenzoate

Ethyl 3-Iodobenzoate

CAS: 58313-23-8

Formula: C₉H₉IO₂

Purity: >98.0%(GC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 276.07

Ref: 3B-I0536

Ethyl 3-iodobenzoate

CAS: 58313-23-8

Formula: C₉H₉IO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 276.0710

Ref: IN-DA00E9J2

Ethyl 3-iodobenzoate

CAS: 58313-23-8

Ethyl 3-iodobenzoate

Formula: C₉H₉IO₂

Purity: >98%

Color and Shape: Pale yellow Liquid

Molecular weight: 276.07103

Ref: 54-OR4534

Ethyl-3-iodobenzoate

CAS: 58313-23-8

Ethyl-3-iodobenzoate

Formula: C₉H₉IO₂

Purity: 98%

Molecular weight: 276.07

Ref: IN-DG128661

Ethyl 3-iodobenzoate

CAS: 58313-23-8

Ethyl 3-iodobenzoate (EIB) is a catalytic reagent that is used in the synthesis of terminal alkynes. It has been shown to be highly reactive with chloride and transmetallates to form ethyl 3-chlorobenzoate. The reaction time between EIB and chloride can be decreased by adding magnesium to the reaction mixture. This reagent also reacts with thymic acid, a synthon for many thiols, forming ethyl 3-thiophenoate. Ethyl 3-iodobenzoate can also act as an affinity label for halides and heterocycles.

Formula: C₉H₉IO₂

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 276.07 g/mol

Ref: 3D-FE22993

Ethyl 3-Iodobenzoate

CAS: 58313-23-8

Formula: C₉H₉IO₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 276.073

Ref: 10-F038712

Ethyl 3-iodobenzoate, min. 98%

CAS: 58313-23-8

Formula: C₉H₉IO₂

Purity: min. 98%

Color and Shape: Colorless to pale-yellow liquid

Molecular weight: 276.07

Ref: 08-06-0099