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519561

Sigma-Aldrich

3-Bromobenzophenone

98%

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About This Item

Linear Formula:
BrC6H4COC6H5
CAS Number:
1016-77-9
Molecular Weight:
261.11
EC Number:
213-808-5
MDL number:
MFCD00672015
UNSPSC Code:
12352100
PubChem Substance ID:
24873916
NACRES:
NA.22

Quality Level

100

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 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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

519561-BULK:
519561-1G:
519561-5G:
519561-VAR:

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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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.
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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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