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Carbazole-9-ethanol

Carbazole-9-ethanol structure

Carbazole-9-ethanol 

structure
  • CAS No:

    1484-14-6

  • Formula:

    C14H13NO

  • Chemical Name:

    Carbazole-9-ethanol

  • Synonyms:

    9H-Carbazole-9-ethanol;Carbazole-9-ethanol;N-(2-Hydroxyethyl)carbazole;N-(Hydroxyethyl)carbazole;N-(β-Hydroxyethyl)carbazole;9-(2-Hydroxyethyl)carbazole;2-(9-Carbazolyl)ethanol;2-(N-Carbazolyl)ethanol;NSC 21081;9-(2-Hydroxyethyl)-9H-carbazole;2-(9H-Carbazol-9-yl)ethanol;2-(9H-Carbazol-9-yl)ethan-1-ol

  • Categories:

    Specialty Chemicals

Carbazole-9-ethanol Basic Attributes

211.264

211.26

604-632-3

21081

DTXSID20281278

2933990090

Characteristics

25.2

2.6

Off-white fluffy crystalline powder

1.17±0.1 g/cm3(Predicted)

79.5-80.5 °C

220 °C @ Press: 5 Torr

204.6±26.5 °C

1.630

1.27E-07mmHg at 25°C

Safety Information

NONH for all modes of transport

3

R36/37/38

26-36

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Carbazole-9-ethanol Use and Manufacturing

16 g of carbazole, 14 g of sodium hydroxide and 7 ml of purified water were mixed with 80 ml of methyl ethyl ketone and the resultant mixture was heated and refluxed under stirring for 30 minutes. While refluxing the mixture, 13 ml of 2-chloroethanol was dropped therein over 1 hour. After refluxing the resultant mixture for additional 3 hours, 8 g of sodium hydroxide was added thereto. While refluxing the resultant mixture, 13 ml of 2-chloroethanol was dropped thereinto over 1 hour. Next, the resultant mixture was refluxed for 24 hours. Then the reaction mixture was cooled to room temperature by allowing to stand, poured into 3 L of purified water and extracted with ether. After removing the ether with an evaporator, the unreacted carbazole was filtered off. From the viscous reaction mixture thus obtained, N-(2-hydroxyethyl)carbazole was isolated by column chromatography (silica gel/benzene). The yield was 20%.

Computed Properties

Molecular Weight:211.26
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:211.099714038
Monoisotopic Mass:211.099714038
Topological Polar Surface Area:25.2
Heavy Atom Count:16
Complexity:221
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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