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Key Documents

519561

Sigma-Aldrich

3-Bromobenzophenone

98%

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About This Item

Linear Formula:
BrC6H4COC6H5
CAS Number:
Molecular Weight:
261.11
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

mp

74.5-77.5 °C (lit.)

SMILES string

Brc1cccc(c1)C(=O)c2ccccc2

InChI

1S/C13H9BrO/c14-12-8-4-7-11(9-12)13(15)10-5-2-1-3-6-10/h1-9H

InChI key

XNUMUNIJQMSNNN-UHFFFAOYSA-N

Related Categories

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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Similar or Totally Different: The Control of Conjugation Degree through Minor Structural Modifications, and Deep-Blue Aggregation-Induced Emission Luminogens for Non-Doped OLEDs.
Huang J, et al.
Advances in Functional Materials, 23(18), 2329-2337 (2013)
Sonovoltammetric measurement of the rates of electrode processes with fast coupled homogeneous kinetics: Making macroelectrodes behave like microelectrodes.
Compton RG, et al.
Chemical Communications (Cambridge, England), 9, 1017-1018 (1996)
Mark F. Mechelke et al.
The Journal of organic chemistry, 64(13), 4821-4829 (2001-10-25)
The synthesis of a family of farnesol analogues, incorporating aromatic rings, has been achieved in high yields through the development of a regioselective coupling of allylic tetrahydropyranyl ethers with organometallic reagents. The allylic THP group is displaced readily by Grignard
Transition-metal catalyzed synthesis of ketoprofen.
Ramminger C, et al.
Journal of the Brazilian Chemical Society, 11(2), 105-111 (2000)

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