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Merck
CN

542121

3′-溴-5′-氯-2′-羟基苯乙酮

97%

别名:

1-(3-溴-5-氯-2-羟基苯基)乙酮, 5-氯-3-溴-2-羟基苯乙酮

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关于此项目

线性分子式:
ClC6H2(Br)(OH)COCH3
化学文摘社编号:
分子量:
249.49
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
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assay

97%

mp

100-103 °C (lit.)

functional group

bromo, chloro, ketone

SMILES string

CC(=O)c1cc(Cl)cc(Br)c1O

InChI

1S/C8H6BrClO2/c1-4(11)6-2-5(10)3-7(9)8(6)12/h2-3,12H,1H3

InChI key

FFAVKFQPEOGJOA-UHFFFAOYSA-N

General description

3′-Bromo-5′-chloro-2′-hydroxyacetophenone is a halogenated aromatic hydroxyl ketone. It participates in the synthesis of racemates of 8-bromo-6-chloro-2-alkyl substituted chroman-4-ones.

Packaging

3′-Bromo-5′-chloro-2′-hydroxyacetophenone (3-bromo-5-chloro-2-hydroxyacetophenone) may be used in the synthesis of corresponding chalcones and structurally related dienones by reacting with appropriate aldehydes.
It may also be used in the preparation of the bioactive 8-bromo-6-chloro-2-substituted 4-chromanone.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Christine Dyrager et al.
Bioorganic & medicinal chemistry, 19(8), 2659-2665 (2011-04-05)
A series of dihalogenated chalcones and structurally related dienones were synthesized and evaluated for their antiproliferative activity in 10 different cancer cell lines and for their effect on microtubule assembly. All compounds showed cytotoxic activity, with IC(50) values in the
Maria Fridén-Saxin et al.
The Journal of organic chemistry, 74(7), 2755-2759 (2009-03-28)
A base-promoted condensation between 2-hydroxyacetophenones and aliphatic aldehydes has been studied. The reaction has been optimized to afford 2-alkyl-substituted 4-chromanones in an efficient manner using microwave heating. Performing the reaction using diisopropylamine in EtOH at 170 degrees C for 1
Proline-mediated formation of novel chroman-4-one tetrahydropyrimidines.
Friden-Saxin M, et al.
Tetrahedron, 68(35), 7035-7040 (2012)



全球贸易项目编号

货号GTIN
542121-25G04061831821079