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277592

Sigma-Aldrich

9-Vinylcarbazole

98%

Synonym(s):

9-Vinyl-9H-carbazole, N-Ethenylcarbazole, N-Vinylcarbazole

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About This Item

Empirical Formula (Hill Notation):
C14H11N
CAS Number:
1484-13-5
Molecular Weight:
193.24
Beilstein:
132988
EC Number:
216-055-0
MDL number:
MFCD00004966
UNSPSC Code:
12162002
PubChem Substance ID:
24856771
NACRES:
NA.23

Assay

98%

bp

154-155 °C/3 mmHg (lit.)

mp

60-65 °C (lit.)

SMILES string

C=Cn1c2ccccc2c3ccccc13

InChI

1S/C14H11N/c1-2-15-13-9-5-3-7-11(13)12-8-4-6-10-14(12)15/h2-10H,1H2

InChI key

KKFHAJHLJHVUDM-UHFFFAOYSA-N

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Related Categories

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 4 Dermal - Aquatic Acute 1 - Aquatic Chronic 1 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Merve Kara et al.
Macromolecular rapid communications, 36(23), 2070-2075 (2015-09-12)
A new phenacyl-type photoinitiator based on ethyl carbazole as a long wavelength photo-initiator is developed for free radical polymerization. Phenacyl ethyl carbazolium hexafluoroantimonate (PECH) photoinitiator is synthesized in a two-step, one-pot manner by quaternizing ethyl carbazole with phenacyl bromide and
Ceren Kütahya et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(46), 10444-10451 (2020-04-29)
NIR exposure at 790 nm activated photopolymerization of monomers comprising UV-absorbing moieties by using [CuII /(TPMA)]Br2 (TPMA=tris(2-pyridylmethyl)amine) in the ppm range and an alkyl bromide as initiator. Some of them comprised structural elements selected either from those showing proton transfer or

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