ChemicalBook--->CAS DataBase List--->17422-33-2

17422-33-2

17422-33-2 Structure

17422-33-2 Structure
IdentificationMore
[Name]

6-Chloroindole
[CAS]

17422-33-2
[Synonyms]

SC 58083
6-CHLOROINDOLE
6-CHLORO-1H-INDOLE
TIMTEC-BB SBB004059
1H-Indole, 6-chloro-
6-Chloroindole, 97+%
1H-Indole,6-chloro-(9CI)
6-chloroindole 17422-32-2
6-chloro-1H-indole(SALTDATA: FREE)
[EINECS(EC#)]

241-449-4
[Molecular Formula]

C8H6ClN
[MDL Number]

MFCD00005681
[Molecular Weight]

151.59
[MOL File]

17422-33-2.mol
Chemical PropertiesBack Directory
[Appearance]

Light Orange Powder
[Melting point ]

87-90 °C (lit.)
[Boiling point ]

248.91°C (rough estimate)
[density ]

1.1976 (rough estimate)
[refractive index ]

1.5437 (estimate)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

slightly soluble
[form ]

Crystalline Powder
[pka]

16.10±0.30(Predicted)
[color ]

Beige
[Water Solubility ]

slightly soluble
[Detection Methods]

HPLC,NMR
[BRN ]

112345
[Stability:]

Store in Refrigerator
[CAS DataBase Reference]

17422-33-2(CAS DataBase Reference)
[NIST Chemistry Reference]

6-Chloroindole(17422-33-2)
Questions And AnswerBack Directory
[Synthesis]

Synthesis of 17422-33-2
6.6 g of 4-chloro-2-nitrotoluene (compound 1c, 0.039 mol) and 23.0 g of DMFDMA (0.193 mol, 5 eq) were added to acetonitrile (80 mL). The reaction temperature was raised to 85 °C–95 °C and refluxed for 5 hours. The reaction was cooled, the solvent was evaporated to dryness, and the product was washed with water and a trace amount of ethanol to give 8.4 g of crude product 2c (0.0369 mol, yield 94.6%).
The obtained intermediate 2c was added to 118 mL of methanol containing 10 wt% hydrazine (hydrazine content 0.36 mol, 10 eq), and the temperature was raised to 50 °C. The reaction was carried out for 8 hours and then cooled to room temperature. The solvent was evaporated to dryness to give 5.4 g of product 3C,6-chloroindole (0.0355 mol, yield 96.3%).

Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

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

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[Hazard Note ]

Irritant
[TSCA ]

A
[HS Code ]

29339900
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

6-Chloro-1H-indole(17422-33-2).msds
Hazard InformationBack Directory
[Chemical Properties]

Light Orange Powder
[Uses]

6-Chloroindole (cas# 17422-33-2) is a compound useful in organic synthesis.
[Definition]

ChEBI: 6-Chloroindole is a member of indoles.
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 55, p. 580, 1990 DOI: 10.1021/jo00289a036
[General Description]

6-Chloroindole, when added to Claviceps purpurea, produced the corresponding substituted L-tryptophan.
Spectrum DetailBack Directory
[Spectrum Detail]

6-Chloroindole(17422-33-2)MS
6-Chloroindole(17422-33-2)1HNMR
6-Chloroindole(17422-33-2)13CNMR
6-Chloroindole(17422-33-2)IR1
6-Chloroindole(17422-33-2)IR2
6-Chloroindole(17422-33-2)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

6-Chloroindole, 99%(17422-33-2)
[Alfa Aesar]

6-Chloroindole, 99%(17422-33-2)
[Sigma Aldrich]

17422-33-2(sigmaaldrich)
[TCI AMERICA]

6-Chloroindole,>98.0%(GC)(17422-33-2)
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