Skip to Content
Merck
CN
All Photos(2)

Documents

329681

Sigma-Aldrich

3,5-Dibromotoluene

97%

Sign Into View Organizational & Contract Pricing

Linear Formula:
CH3C6H3Br2
CAS Number:
Molecular Weight:
249.93
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

bp

246 °C (lit.)

mp

34-38 °C (lit.)

SMILES string

Cc1cc(Br)cc(Br)c1

InChI

1S/C7H6Br2/c1-5-2-6(8)4-7(9)3-5/h2-4H,1H3

InChI key

DPKKOVGCHDUSAI-UHFFFAOYSA-N

General description

3,5-Dibromotoluene is a halogenated toluene and its electric moment was evaluated.

Application

3,5-Dibromotoluene was used in the preparation of 3,5-bis(diphenylphosphinothioyl)toluene.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

235.4 °F

Flash Point(C)

113 °C

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

Synthesis, molecular structure, and photoluminescence properties of palladium and platinum complexes containing phosphine sulfide-based SCS pincer ligand.
Kanbara T and Yamamoto T.
Journal of Organometallic Chemistry, 688(1), 15-19 (2003)
The Electric Moments of Morpholine and Some Halogenated Toluenes1.
Maryott AA, et al.
Journal of the American Chemical Society, 62(9), 2320-2324 (1940)
Asami Yoshii et al.
Chemistry, an Asian journal, 15(14), 2181-2186 (2020-05-26)
Oligo-meta-phenylenes have been designed and synthesized as multipotent base materials of single-layer organic light-emitting devices. Simple molecular structures of oligo-meta-phenylenes composed of linear phenylene arrays benefited from the wealth of modern reactions available for biaryl couplings and were concisely synthesized

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