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36684-65-8

36684-65-8 Structure

36684-65-8 Structure
IdentificationBack Directory
[Name]

6-CHLORO-1 2 3 4-TETRAHYDROCARBAZOLE 9&
[CAS]

36684-65-8
[Synonyms]

NSC 298291
1,2,3,4-Tetrahydro-6-chlorocarbazole
6-CHLORO-1 2 3 4-TETRAHYDROCARBAZOLE 9&
6-Chloro-1,2,3,4-tetrahydrocarbazole >
1H-Carbazole, 6-chloro-2,3,4,9-tetrahydro-
6-CHLORO-1,2,3,4-TETRAHYDROCARBAZOLE, 98 %
[Molecular Formula]

C12H12ClN
[MDL Number]

MFCD00541331
[MOL File]

36684-65-8.mol
[Molecular Weight]

205.683
Chemical PropertiesBack Directory
[Melting point ]

145-148 °C(lit.)
[Boiling point ]

358.8±37.0 °C(Predicted)
[density ]

1.280
[storage temp. ]

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

slightly sol. in Methanol
[form ]

powder to crystal
[pka]

16.93±0.20(Predicted)
[color ]

White to Light yellow
[λmax]

292nm(ethylene glycol)(lit.)
[InChI]

InChI=1S/C12H12ClN/c13-8-5-6-12-10(7-8)9-3-1-2-4-11(9)14-12/h5-7,14H,1-4H2
[InChIKey]

CNQQPGJXOHSTQR-UHFFFAOYSA-N
[SMILES]

N1C2=C(C=C(Cl)C=C2)C2=C1CCCC2
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2933.99.8290
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Spectrum DetailBack Directory
[Spectrum Detail]

6-CHLORO-1 2 3 4-TETRAHYDROCARBAZOLE 9&(36684-65-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Chlorophenylhydrazine hydrochloride

1073-70-7

Cyclohexanone

108-94-1

6-CHLORO-1 2 3 4-TETRAHYDROCARBAZOLE  9&

36684-65-8

GENERAL METHODS: Cyclohexanone (0.91 g, 10.0 mmol) was mixed with bis(trifluoromethanesulfonyl)imide salt ([(HSO3-p)2im][CF3SO3]) (0.5 mmol) in deionized water (15 mL), followed by the addition of p-chlorophenylhydrazine hydrochloride (1.44 g, 10.0 mmol). The reaction mixture was placed in a microwave reactor and stirred at 100 °C for about 15 min, and the reaction process was monitored by gas chromatography-mass spectrometry (GC-MS). After completion of the reaction, the mixture was cooled to room temperature and the precipitate was collected by filtration to afford 6-chloro-1,2,3,4-tetrahydrocarbazole. The mixed system of [(HSO3-p)2im][CF3SO3]/H2O used in the reaction can be directly recycled for subsequent reactions.

[References]

[1] Journal of Fluorine Chemistry, 2012, vol. 144, p. 45 - 50,6
[2] Tetrahedron Letters, 2018, vol. 59, # 22, p. 2145 - 2149
[3] Heterocyclic Communications, 2003, vol. 9, # 1, p. 9 - 12
[4] Organic and Biomolecular Chemistry, 2016, vol. 14, # 41, p. 9868 - 9873
[5] Patent: CN105968039, 2016, A. Location in patent: Paragraph 0049-0051
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