Skip to Content
Merck

479748

Sigma-Aldrich

9H-Carbazole-9-ethanol

95%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C14H13NO
CAS Number:
Molecular Weight:
211.26
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Pricing and availability is not currently available.

Quality Level

Assay

95%

mp

78-82 °C (lit.)

SMILES string

OCCn1c2ccccc2c3ccccc13

InChI

1S/C14H13NO/c16-10-9-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,16H,9-10H2

InChI key

IIKVAWLYHHZRGV-UHFFFAOYSA-N

General description

9H-Carbazole-9-ethanol (ECOH) is a carbazole derivative.

Application

9H-Carbazole-9-ethanol may be used to synthesize 2-(9H-carbazol-9-yl)ethyl methacrylate.[1][2][3]

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Thermal aging of single-layer polymer light-emitting diodes composed of a carbazole and oxadiazole containing copolymer doped with singlet or triplet emitters.
Rungta P, et al.
Synthetic Metals, 160(23), 2486-2493 (2010)
Rukiye Ayranci et al.
The Analyst, 142(18), 3407-3415 (2017-08-22)
Herein, we report the synthesis and characterization of a new rhodamine-based monomer (RD-CZ), and an investigation of the optical and electrochemical properties of the corresponding polymer (P(RD-CZ)), which was electropolymerized on an ITO electrode. The resulting P(RD-CZ) polymer film was
Synthesis and photophysical properties of a poly (methyl methacrylate) polymer with carbazolyl side groups.
Martins TD, et al.
Journal of the Brazilian Chemical Society, 19(8), 1450-1461 (2008)
Yifen Lin et al.
Food chemistry, 264, 1-8 (2018-06-02)
Disassembly of cell wall polysaccharides accompanied with softening is very common in harvested fruits. To develop a facile postharvest approach, which can be used at ambient temperature, for suppressing softening and maintaining higher nutritive cell wall polysaccharides of Younai plums
Poly(methyl methacrylate)copolymers containing pendant carbazole and oxadiazole moieties for applications in single-layer organic light emitting devices.
Evanoff DD, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 46(23), 7882-7897 (2008)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service