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479748

Sigma-Aldrich

9H-Carbazole-9-ethanol

95%

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About This Item

Empirical Formula (Hill Notation):
C14H13NO
CAS Number:
1484-14-6
Molecular Weight:
211.26
MDL number:
MFCD00518704
UNSPSC Code:
12352100
PubChem Substance ID:
24871644
NACRES:
NA.22

Quality Level

100

Assay

95%

mp

78-82 °C (lit.)

functional group

hydroxyl

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

Related Categories

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

479748-5G:
479748-VAR:
479748-BULK:
479748-25G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCK9067
MKBR7966V
MKBH9196V
85796KJ
12101BJ

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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)

Global Trade Item Number

SKUGTIN
479748-5G4061833547847
479748-25G4061833547830

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