ChemicalBook Product Catalog Chemical Reagents Organic reagents Esters Ethyl compound Ethyl 4-iodobenzoate

Ethyl 4-iodobenzoate

Ethyl 4-iodobenzoate Basic information
Product Name:Ethyl 4-iodobenzoate
Synonyms:RARECHEM AL BI 0710;ETHYL 4-IODOBENZOATE;ETHYL P-IODOBENZOATE;IBE;LABOTEST-BB LT01148245;ETHYL 4-IODOBENZENE;4-IODOBENZONIC ACID ETHYL ESTER;4-IODOBENZOIC ACID ETHYL ESTER
CAS:51934-41-9
MF:C9H9IO2
MW:276.07
EINECS:429-550-3
Product Categories:Aromatics;Aromatic Esters;Miscellaneous Reagents;Acids & Esters;Iodine Compounds;C8 to C9;Carbonyl Compounds;Esters;Pharmaceutical Intermediates
Mol File:51934-41-9.mol
Ethyl 4-iodobenzoate Structure
Ethyl 4-iodobenzoate Chemical Properties
Melting point 267 °C
Boiling point 281-283 °C
density 1.641 g/mL at 25 °C (lit.)
refractive index n20/D 1.5880(lit.)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform, Dichloromethane, Ethyl Acetate, Hexane
form Liquid
Specific Gravity1.66
color Clear colorless to yellow
Water Solubility insoluble
Sensitive Light Sensitive
BRN 2208568
CAS DataBase Reference51934-41-9(CAS DataBase Reference)
NIST Chemistry ReferenceEthyl 4-iodobenzoate(51934-41-9)
Safety Information
Hazard Codes N,Xi,C
Risk Statements 51/53-36/37/38
Safety Statements 61-24/25
RIDADR UN 3082 9/PG 3
WGK Germany 3
F 8
Hazard Note Irritant
HazardClass IRRITANT, LIGHT SENSITIVE
HS Code 29163990
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Ethyl 4-iodobenzoate Usage And Synthesis
Chemical PropertiesLight Yellow Oil
UsesEthyl 4-iodobenzoate can be used in the synthesis of biphenyl derivatives via Negishi cross coupling with the intermediates of the type ArMg(tmp)·2LiCl (tmp = trimethylolpropane). It can also be used as a starting material in the synthesis of p-carbomethoxyphenylmagnesium bromide, a polyfunctional organometallic reagent that can be used as building block in the synthesis of complex target molecules.
Ethyl 4-iodobenzoate Preparation Products And Raw materials
Preparation Products4-ETHYNYL-BENZOIC ACID-->ETHYL 4-(5-FORMYL-2-FURYL)BENZOATE-->DIETHYL BIPHENYL-4,4'-DICARBOXYLATE-->4-(TRIMETHYLSILYLETHYNYL)BENZYL ALCOHOL-->ETHYL 4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZOATE-->4-ETHYNYLBENZYL ALCOHOL 97-->4-(2-OXO-PROPYL)-BENZOIC ACID ETHYL ESTER-->Ethyl 4-etoxybenzoate-->Ethyl benzoate-->ETHYL 4-ACETYLBENZOATE-->4'-CARBOETHOXY-2,2,2-TRIFLUOROACETOPHENONE-->4-CARBOETHOXYPHENYL CYCLOPENTYL KETONE
1-methyl-2-(1-piperidinyl)ethyl 2-iodobenzoate ETHYL 2-ETHOXY-4-IODOBENZOATE ETHYL 3-HYDROXY-4-IODOBENZOATE TETRAIODOBENZOIC ACID, BUTYL ESTER 2-(dimethylamino)ethyl 2-iodobenzoate 2-(7-NITRO-3-OXO-3,4-DIHYDRO-2H-1,4-BENZOXAZIN-2-YL)ETHYL 4-IODOBENZENECARBOXYLATE Ethyl 4-iodo-3-methoxybenzoate ETHYL 2-IODOBENZOATE,ETHYL O-IODOBENZOATE 1,2-BENZENEDICARBOXYLIC ACID,4-IODO-,1,2-DIETHYL ESTER 1,3-THIAZOL-5-YLMETHYL 4-IODOBENZENECARBOXYLATE (2-CHLORO-1,3-THIAZOL-5-YL)METHYL 4-IODOBENZENECARBOXYLATE ETHYL 4-IODOBENZOATE, (4-IODOBENZOIC ACID ETHYL ESTE ETHYL 2-IODOBENZOATE, (2-IODOBENZOIC ACID ETHYL ESTER) ETHYL4-IODOBENZOATE,(4-IODOBENZOICACIDETHYL ESTER) BUTTPARK 88\11-83 4-IODO-3-NITRO-BENZOIC ACID ETHYL ESTER 3-ACETAMINO-2,4,6-TRIIODOBENZOIC ACID ETHYL ESTER ETHYL 3-IODOBENZOATE, (3-IODOBENZOIC ACID ETHYL ESTER
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