ChemicalBook--->CAS DataBase List--->27034-51-1

27034-51-1

27034-51-1 Structure

27034-51-1 Structure
IdentificationMore
[Name]

6-Chloroindole-2-carboxylic acid ethyl ester
[CAS]

27034-51-1
[Synonyms]

6-CHLOROINDOLE-2-CARBOXYLIC ACID ETHYL ESTER
SPECS AP-283/40634148
6-Chloroindole-2-Carboxylic Acid Ethyl Acid
Ethyl 6-chloroindole-2-carboxylate
6-CHLORO-2-INDOLECARBOXYLIC METHYL ESTER
Ethyl 6-Chloroindole-2-Carboxylicate
6-CHLORO-2-INDOLECARBOXYLIC
6-Chloroindole-2-carboxylic acid ethyl ester ,99%
[Molecular Formula]

C11H10ClNO2
[MDL Number]

MFCD03084731
[Molecular Weight]

223.66
[MOL File]

27034-51-1.mol
Chemical PropertiesBack Directory
[Melting point ]

169-171 °C
[Boiling point ]

375.0±22.0 °C(Predicted)
[density ]

1.329±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

Solid
[pka]

14.11±0.30(Predicted)
[Appearance]

Light brown to gray Solid
[Detection Methods]

HPLC
[CAS DataBase Reference]

27034-51-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933998090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Hydrochloric acid-->Diethyl ether-->Acetic acid-->Diethyl oxalate-->Potassium-->4-Chloro-2-nitrotoluene-->Ethyl 3-(4-chloro-2-nitrophenyl)-2-oxopropanoate-->(Z)-4-(4-Chlorobenzylidene)-2-methyloxazol-5(4H)-one-->ethyl 2-ethoxy acrylate-->3-Chlorophenylhydrazine hydrochloride-->Ethyl-4-Chloroindole-2-Carboxylate-->5-CHLORO-2-IODOANILINE-->4-Chloro-2-nitrobenzaldehyde-->Iron-->3-Chloroaniline
Hazard InformationBack Directory
[Uses]

Ethyl 6-chloroindole-2-carboxylate is an organic compound mainly used as a pharmaceutical intermediate and chemical reagent.
[Synthesis]

2-Propenoic acid, 2-azido-3-(4-chlorophenyl)-, ethyl ester, (2Z)-

24513-05-1

6-Chloroindole-2-carboxylic acid ethyl ester

27034-51-1

General method: 6a-d (9.2 mmol) was dissolved in toluene (150 mL) under nitrogen protection, rhodium(II) acetate dimer (203 mg, 0.46 mmol) was added, and the reaction was heated to reflux for 1-2 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate, 25:1 to 18:1, v/v) to afford the target product ethyl 6-chloroindole-2-carboxylate (7a-d) in 51.7%-58.6% overall yields.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 6, p. 1760 - 1762
[2] Journal of Medicinal Chemistry, 1991, vol. 34, # 4, p. 1283 - 1292
Spectrum DetailBack Directory
[Spectrum Detail]

6-Chloroindole-2-carboxylic acid ethyl ester(27034-51-1)1HNMR
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