Skip to Content
Merck
All Photos(1)

Documents

259004

Sigma-Aldrich

3,6-Dibromocarbazole

97%

Synonym(s):

3,6-Dibromo-9-H-carbazole, 3,6-Dibromo-9H-carbazole

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C12H7Br2N
CAS Number:
6825-20-3
Molecular Weight:
325.00
MDL number:
MFCD00004961
UNSPSC Code:
12352100
PubChem Substance ID:
24855676
NACRES:
NA.22

Assay

97%

form

powder

mp

204-206 °C (lit.)

SMILES string

Brc1ccc2[nH]c3ccc(Br)cc3c2c1

InChI

1S/C12H7Br2N/c13-7-1-3-11-9(5-7)10-6-8(14)2-4-12(10)15-11/h1-6,15H

InChI key

FIHILUSWISKVSR-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Lithiation of 3,6-dibromocarbazole with n-butyllithium has been studied.

Application

3,6-Dibromocarbazole has been used in the preparation of N-(2-hydroxyethyl)-3,6-dibromocarbazole.

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

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’.

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

Slide 1 of 1

1 of 1

Carbazole VETRANAL®, analytical standard

Supelco

46100

Carbazole

A useful procedure for diiodination of carbazoles and subsequent efficient transformation to novel 3, 6-bis (triethoxysilyl) carbazoles giving mesoporous materials.
Maegawa Y, et al.
Tetrahedron Letters, 47(39), 6957-6960 (2006)
New NLO stilbene derivatives bearing phosphonate ester electron-withdrawing groups.
Belfield KD, et al.
Tetrahedron Letters, 38(35), 6131-6134 (1997)
Yan Wu et al.
Environmental science & technology, 52(8), 4536-4545 (2018-03-23)
Polyhalogenated carbazoles (PHCZs) were recently discovered in Great Lakes sediment and other aquatic systems. However, knowledge about their bioaccumulation and potential risks to fish and wildlife remains very limited. The present study investigated PHCZs in Great Lakes lake trout (
Li Fang et al.
Ecotoxicology and environmental safety, 184, 109609-109609 (2019-09-14)
Carbazole and halogenated carbazoles have been widely detected throughout the environment in soil, river deposits, and lake sediments. Human exposure to these compounds may occur through inhalation, drinking water, dietary intake and/or skin contact, and exposure levels in the body
Yanqiu Chen et al.
Environmental pollution (Barking, Essex : 1987), 232, 264-273 (2017-09-28)
Polyhalogenated carbazoles (PHCs) are a class of emerging organic contaminants that have received increasing concern due to their widespread distribution and dioxin-like toxicity. Although previous studies have suggested possible natural sources of PHCs in the environment, the formation pathways are
View All Related Papers

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