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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

Quality Level

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

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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
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)
Transition-metal catalyzed synthesis of ketoprofen.
Ramminger C, et al.
Journal of the Brazilian Chemical Society, 11(2), 105-111 (2000)
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)

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