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2-Bromotoluene | CAS:95-46-5
2-Bromotoluene
  • Name:2-Bromotoluene
  • CAS:95-46-5
  • Synonyms:1-Bromo-2-methylbenzene; o-Bromomethylbenzene; 2-Methylbromobenzene; o-Methylphenyl bromide; o-Tolylbromide
  • Molecular Formula:C7H7Br
  • Molecular Weight:171.04
  • EINESC:202-421-7

Description

Properties

Melting point -27 ºC
Boiling point 181.5 ºC
Flash point 78 ºC
Density 1.423
Refractive index 1.555-1.557

Safety

Symbol(GHS) Xn
Hazard Codes R22;R36/37/38
SDS/MSDS S26;S37/39

SDS

Source SDS/MSDS Samples
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Articles
Peer-Reviewed Papers
A novel "pro-sensitizer" based sensing of enzymes using Tb(III) luminescence in a hydrogel matrix.Sandip Bhowmik et al.Chemical communications (Cambridge, England), 48(38), 4624-4626 (2012-04-03) Family 18 chitolectins: comparison of MGP40 and HUMGP39.Zaheer-ul-Haq et al.Biochemical and biophysical research communications, 359(2), 221-226 (2007-06-05) The syntheses and characterizations of molybdenum(VI) complexes with catechol and 2,3-dihydroxynaphthalene, and the structure-effect relationship in their in vitro anticancer activities.Jun Feng et al.Dalton transactions (Cambridge, England : 2003), 41(28), 8697-8702 (2012-06-14) Hydrolytic metal with a hydrophobic periphery: titanium(IV) complexes of naphthalene-2,3-diolate and interactions with serum albumin.Arthur D Tinoco et al.Inorganic chemistry, 47(18), 8380-8390 (2008-08-20) Phase II metabolism in human skin: skin explants show full coverage for glucuronidation, sulfation, N-acetylation, catechol methylation, and glutathione conjugation.Nenad Manevski et al.Drug metabolism and disposition: the biological fate of chemicals, 43(1), 126-139 (2014-10-24) [The synthesis, 1H NMR and IR study of [(n-Bu)4N]2[Mo2O5(OC10H6O)2] and [(n-Bu)4N]2[Mo4O10 (OC10H6O)2(OCH3)2]].Xiao-ming Lu et al.Guang pu xue yu guang pu fen xi = Guang pu, 22(1), 36-38 (2003-08-28) Regulation of rat liver phenylalanine hydroxylase. I. Kinetic properties of the enzyme's iron and enzyme reduction site.R Shiman et al.The Journal of biological chemistry, 269(40), 24637-24646 (1994-10-07) Synthesis and properties of butterfly-shaped expanded naphthofuran derivatives.Kentaro Nakanishi et al.The Journal of organic chemistry, 79(6), 2625-2631 (2014-02-26) Reactions of linoleic acid peroxyl radicals with phenolic antioxidants: a pulse radiolysis study.M Erben-Russ et al.International journal of radiation biology and related studies in physics, chemistry, and medicine, 52(3), 393-412 (1987-09-01) Terminal group effects on the fluorescence spectra of europium(III) nitrate complexes with a family of amide-based 2,3-dihydroxynaphthalene derivatives.Ke-Wei Lei et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 65(1), 187-190 (2006-03-10) Chemical speciation of iron in seawater by cathodic stripping voltammetry with dihydroxynaphthalene.Constant M G van den Berg Analytical chemistry, 78(1), 156-163 (2005-12-31) Synthesis of bis (ether anhydride) s for poly (ether imide) s having 1, 2-linked units by nitrodisplacement with catechol derivatives. Eastmond GC and Paprotny J. Macromolecules, 28(7), 2140-2146 (1995) Surface modification of anatase nanoparticles with fused ring catecholate type ligands: a combined DFT and experimental study of optical properties.Tatjana D Savić et al.Nanoscale, 4(5), 1612-1619 (2012-02-09) The multidrug efflux regulator TtgV recognizes a wide range of structurally different effectors in solution and complexed with target DNA: evidence from isothermal titration calorimetry.María-Eugenia Guazzaroni et al.The Journal of biological chemistry, 280(21), 20887-20893 (2005-03-16) Redox cycling by cytochrome P-450.P Besse et al.Biochemical Society transactions, 25(4), S579-S579 (1998-02-05) Tris(spiroborate)-type anionic nanocycles.Hiroshi Danjo et al.Chemistry, an Asian journal, 7(7), 1529-1532 (2012-04-11) Application of cyclophosphazene derivatives as flame retardants for ABS.Shin YJ, et al. Journal of Industrial and Engineering Chemistry (Amsterdam, Netherlands), 16(3), 364-367 (2010) Copper (I)-catalyzed asymmetric oxidative coupling polymerization of 2, 3-dihydroxynaphthalene using bisoxazoline ligands. Habaue S, et al. Macromolecules, 36(8), 2604-2608 (2003)
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