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Key Documents

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Safety Information

360082

Sigma-Aldrich

2-Phenylbenzyl bromide

97%

Synonym(s):

2-(Bromomethyl)biphenyl

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100 EA
¥539.87

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100 EA
¥539.87

About This Item

Linear Formula:
C6H5C6H4CH2Br
CAS Number:
19853-09-9
Molecular Weight:
247.13
MDL number:
MFCD00075454
UNSPSC Code:
12352100
PubChem Substance ID:
24862143
NACRES:
NA.22

¥539.87

Please contact Customer Service for Availability
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Assay

97%

form

liquid

refractive index

n20/D 1.6280 (lit.)

bp

120-125 °C/0.1 mmHg (lit.)

density

1.353 g/mL at 25 °C (lit.)

functional group

bromo
phenyl

SMILES string

BrCc1ccccc1-c2ccccc2

InChI

1S/C13H11Br/c14-10-12-8-4-5-9-13(12)11-6-2-1-3-7-11/h1-9H,10H2

InChI key

SEXZHJJUKFXNDY-UHFFFAOYSA-N

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Certified Vial Kit, Low Adsorption (LA), 2 mL, pk of 100 volume 2 mL, clear glass vial (with marking spot), natural PTFE/silicone septa, thread for 9 mm

29651U

Certified Vial Kit, Low Adsorption (LA), 2 mL, pk of 100

Certified Vial Kit, Low Adsorption (LA), 2 mL, pk of 100 volume 2 mL, clear glass vial (with marking spot), natural PTFE/silicone septa (with slit), thread for 9 mm

29652U

Certified Vial Kit, Low Adsorption (LA), 2 mL, pk of 100

Certified Vial Kit, Low Adsorption (LA), 2 mL, pk of 100 volume 2 mL, amber glass vial (with marking spot), natural PTFE/silicone septa, thread for 9 mm

29653U

Certified Vial Kit, Low Adsorption (LA), 2 mL, pk of 100

Certified Vial Kit, Low Adsorption (LA), 2 mL, pk of 100 volume 2 mL, amber glass vial (with marking spot), natural PTFE/silicone septa (with slit), thread for 9 mm

29654U

Certified Vial Kit, Low Adsorption (LA), 2 mL, pk of 100

feature

closure type screw top vial

feature

closure type screw top vial

feature

closure type screw top vial

feature

closure type screw top vial

material

clear glass vial (with marking spot), natural PTFE/silicone septa, light blue polypropylene cap (Mass Spec quality)

material

clear glass vial (with marking spot), light blue polypropylene cap (Mass Spec quality), natural PTFE/silicone septa (with slit)

material

amber glass vial (with marking spot), light blue polypropylene cap (Mass Spec quality), natural PTFE/silicone septa

material

amber glass vial (with marking spot), light blue polypropylene cap (Mass Spec quality), natural PTFE/silicone septa (with slit)

fitting

thread for 9 mm

fitting

thread for 9 mm

fitting

thread for 9 mm

fitting

thread for 9 mm

compatibility

for use with Agilent/HP, for use with Waters

compatibility

for use with Agilent/HP, for use with Thermo Fisher, for use with Waters

compatibility

for use with Agilent/HP, for use with Thermo Fisher, for use with Waters

compatibility

for use with Agilent/HP, for use with Thermo Fisher, for use with Waters

packaging

pkg of 100 ea

packaging

pkg of 100 ea

packaging

pkg of 100 ea

packaging

pkg of 100 ea

General description

2-Phenylbenzyl bromide is a halogenated hydrocarbon.

Application

2-Phenylbenzyl bromide may be used in the synthesis of a parent skeleton of 9H-fluorene.[1]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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    Certificates of Analysis (COA)

    Lot/Batch Number
    1437541V
    1437541
    09121PD
    05205KD
    19215HO

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    Seung Jun Hwang et al.
    Organic letters, 11(20), 4588-4591 (2009-09-17)
    A facile protocol for the Pd-catalyzed preparative synthesis of fluorene derivatives has been developed. While a wide range of fluorenes were easily obtained with high efficiency and selectivity under mild conditions, excellent functional group tolerance was also demonstrated. On the
    Hayrettin O Gülcan et al.
    Archiv der Pharmazie, 348(1), 55-61 (2015-01-13)
    The current structure-activity relationship of profens (i.e., 2-arylpropionic acid derivatives, a class of non-steroidal anti-inflammatory drugs) discusses the importance of α-monomethyl substitution on these compounds, since the activities obtained through their corresponding arylacetic acid derivatives (i.e., α-demethylated derivatives) or α,α-dimethyl-substituted

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