Skip to Content
Merck
All Photos(1)

Documents

125911

Sigma-Aldrich

α,α′-Dibromo-m-xylene

97%

Synonym(s):

1,3-Bis(bromomethyl)benzene, m-Xylylene dibromide

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

About This Item

Linear Formula:
C6H4(CH2Br)2
CAS Number:
626-15-3
Molecular Weight:
263.96
Beilstein:
971085
EC Number:
210-931-6
MDL number:
MFCD00000178
UNSPSC Code:
12352100
PubChem Substance ID:
24847686
NACRES:
NA.22

Assay

97%

form

solid

bp

135-140 °C/20 mmHg (lit.)

mp

74-77 °C (lit.)

SMILES string

BrCc1cccc(CBr)c1

InChI

1S/C8H8Br2/c9-5-7-2-1-3-8(4-7)6-10/h1-4H,5-6H2

InChI key

OXHOPZLBSSTTBU-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

α,α′-Dibromo-m-xylene can cross-link and cyclize peptides containing two cysteine residues.

Application

α,α′-Dibromo-m-xylene has been used in preparation of four novel dinuclear half-titanocenes with meta- and orthoxylene bridges as new metallocenes. It was used in the synthesis of dissymmetrical bis-macrocyclic salt.

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

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

WGK

WGK 3

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

Preparation of new dinuclear half-titanocene complexes with ortho- and meta-xylene linkages and investigation of styrene polymerization.
Linh NTB, et al.
Journal of Organometallic Chemistry, 694(21), 3438-3443 (2009)
Florian P Seebeck et al.
Journal of the American Chemical Society, 128(22), 7150-7151 (2006-06-01)
Dehydroalanine is a nonproteinogenic amino acid, but it is a component of a wide variety of natural products with therapeutic activities. Indeed, this alpha,beta-unsaturated residue is a highly versatile building block due to its rigidifying effect on peptide backbones and
Bis-aminals: efficient tools for bis-macrocycle synthesis.
Le Baccon M, et al.
New. J. Chem., 25(9), 1168-1174 (2001)

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