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
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
97%
mp
100-103 °C (lit.)
官能团
bromo
chloro
ketone
SMILES字符串
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
一般描述
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.
包装
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.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Proline-mediated formation of novel chroman-4-one tetrahydropyrimidines.
Friden-Saxin M, et al.
Tetrahedron, 68(35), 7035-7040 (2012)
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
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