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1075-35-0

1075-35-0 Structure

1075-35-0 Structure
IdentificationMore
[Name]

5-CHLORO-2-METHYLINDOLE
[CAS]

1075-35-0
[Synonyms]

2-METHYL-5-CHLOROINDOLE
5-CHLORO-2-METHYLINDOLE
RARECHEM AH BS 0087
TIMTEC-BB SBB003903
5-CHLORO-2-METHYLINDOLE 97%
2-Methyl-5-chloro-1H-indole
[EINECS(EC#)]

214-052-9
[Molecular Formula]

C9H8ClN
[MDL Number]

MFCD00005619
[Molecular Weight]

165.62
[MOL File]

1075-35-0.mol
Chemical PropertiesBack Directory
[Appearance]

light pink to beige-pale brown crystalline powder
[Melting point ]

112-118 °C
[Boiling point ]

140 °C / 0.1mmHg
[density ]

1.1705 (rough estimate)
[refractive index ]

1.5390 (estimate)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

powder to crystal
[pka]

16.66±0.30(Predicted)
[color ]

White to Gray to Brown
[InChIKey]

WUVWAXJXPRYUME-UHFFFAOYSA-N
[CAS DataBase Reference]

1075-35-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

29339980
Hazard InformationBack Directory
[Chemical Properties]

light pink to beige-pale brown crystalline powder
[Uses]

2-Methyl-5-chloroindole has been shown to depress brainstem and telencephalon serotonin for 3 days after 24 hours of being administered intraventricularly.Dyes and metabolites.
[Synthesis Reference(s)]

Journal of the American Chemical Society, 96, p. 5495, 1974 DOI: 10.1021/ja00824a028
[Synthesis]

2-Propanone, 1-(5-chloro-2-nitrophenyl)-

81327-26-6

5-CHLORO-2-METHYLINDOLE

1075-35-0

In a 100 mL stainless steel autoclave, 1.09 g (5.1 mmol) of 5-chloro-2-nitrophenylacetone and 72 mg (4 mol%) of cyclopentadienyl ferric dicarbonyl (dimer) were added as a catalyst and 40 g of toluene as a solvent, and the system was protected by nitrogen. After displacing the atmosphere in the reactor three times (10 kgf/cm2 nitrogen each time), carbon monoxide gas was injected to a pressure of 30 kgf/cm2. The reaction mixture was stirred at 120 °C for 5 h. The reaction was completed by cooling to room temperature. Upon completion of the reaction, it was cooled to room temperature and the complete conversion of 5-chloro-2-nitrophenylacetone was confirmed by liquid chromatography analysis. Subsequently, the reaction mixture was post-treated and purified by silica gel column chromatographic separation to afford 0.79 g (94.0% yield) of the target product 5-chloro-2-methylindole.

[References]

[1] Patent: US2007/83053, 2007, A1. Location in patent: Page/Page column 7
Spectrum DetailBack Directory
[Spectrum Detail]

5-CHLORO-2-METHYLINDOLE(1075-35-0)1HNMR
5-CHLORO-2-METHYLINDOLE(1075-35-0)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

5-Chloro-2-methylindole, 95%(1075-35-0)
[Alfa Aesar]

5-Chloro-2-methylindole, 98%(1075-35-0)
[Sigma Aldrich]

1075-35-0(sigmaaldrich)
[TCI AMERICA]

5-Chloro-2-methylindole,>98.0%(GC)(T)(1075-35-0)
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