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%
产品名称
3′-溴-5′-氯-2′-羟基苯乙酮, 97%
InChI
1S/C8H6BrClO2/c1-4(11)6-2-5(10)3-7(9)8(6)12/h2-3,12H,1H3
SMILES string
CC(=O)c1cc(Cl)cc(Br)c1O
InChI key
FFAVKFQPEOGJOA-UHFFFAOYSA-N
assay
97%
mp
100-103 °C (lit.)
functional group
bromo
chloro
ketone
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.
It may also be used in the preparation of the bioactive 8-bromo-6-chloro-2-substituted 4-chromanone.
signalword
Warning
hcodes
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
新产品
此项目有
Maria Fridén-Saxin et al.
Journal of medicinal chemistry, 55(16), 7104-7113 (2012-07-04)
A series of substituted chromone/chroman-4-one derivatives has been synthesized and evaluated as novel inhibitors of SIRT2, an enzyme involved in aging-related diseases, e.g., neurodegenerative disorders. The analogues were efficiently synthesized in a one-step procedure including a base-mediated aldol condensation using
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)
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