935-99-9 (2-溴-5-氯苯乙酮,1-(2-bromo-5-chlorophenyl)ethan-1-one)

CAS号:
935-99-9
中文名称:
2-溴-5-氯苯乙酮
英文名称:
1-(2-bromo-5-chlorophenyl)ethan-1-one
分子式:
C8H6BrClO
分子量:
233.489640712738

2-溴-5-氯苯乙酮(935-99-9)名称与标识符

名称

中文别名:
1-(2-溴-5-氯苯基)乙酮;2-溴-5-氯苯乙酮;2'-溴-5'-氯苯乙酮;
英文别名:
1-(2-Bromo-5-chlorophenyl)ethanone;2-Acetyl-1-bromo-4-chlorobenzene;2-Bromo-5-chloroacetophenone;1-(2-bromo-5-chlorophenyl)ethan-1-one;2'-BROMO-5'-CHLOROACETOPHENONE;PubChem23873;BCQAWQMDMPBDBW-UHFFFAOYSA-N;CL8884;LS11579;Ethanone, 1-(2-bromo-5-chlorophenyl)-;BC004983;AM806605;AB0027754;W9625;ST24020993;1-(2-Bromo-5-chlorophenyl)ethanone (ACI);Acetophenone, 2′-bromo-5′-chloro- (7CI, 8CI);2′-Bromo-5′-chloroacetophenone;SCHEMBL3121226;GS-3929;CS-0031412;MFCD11847057;SY067370;DTXSID40500054;2 inverted exclamation mark -Bromo-5 inverted exclamation mark -chloroacetophenone;DB-362698;935-99-9;EN300-1912878;AKOS015919676;

标识符

MDL:
MFCD11847057
InChIKey:
BCQAWQMDMPBDBW-UHFFFAOYSA-N
Inchi:
1S/C8H6BrClO/c1-5(11)7-4-6(10)2-3-8(7)9/h2-4H,1H3
SMILES:
O=C(C)C1C(Br)=CC=C(Cl)C=1

2-溴-5-氯苯乙酮(935-99-9)物化性质

实验特性

  • 折射率 : 1.5517 (589.3 nm 15 ºC)
  • 溶解度 : Very 微溶 (0.18 g/L) (25 ºC),
  • 密度 : 1.566±0.06 g/cm3 (20 ºC 760 Torr),

计算特性

  • 精确分子量 : 231.92906g/mol
  • 氢键供体数量 : 0
  • 氢键受体数量 : 1
  • 可旋转化学键数量 : 1
  • 同位素质量 : 231.92906g/mol
  • 重原子数量 : 11
  • 复杂度 : 160
  • 同位素原子数量 : 0
  • 确定原子立构中心数量 : 0
  • 不确定原子立构中心数量 : 0
  • 确定化学键立构中心数量 : 0
  • 不确定化学键立构中心数量 : 0
  • 共价键单元数量 : 1
  • 疏水参数计算参考值(XlogP) : 2.9
  • 拓扑分子极性表面积 : 17.1

2-溴-5-氯苯乙酮(935-99-9)推荐厂家 更多厂家(21)

公司名称手机号/电话联系人QQ微信询单
上海源叶生物科技有限公司 15026964105
15026964105
汤思磊 2881489226
询单
上海瀚思化工有限公司 18939883912
021-34536277
顾经理 3003949364
询单
上海一基实业有限公司 13311756131
021-60548336 QQ:2355265332 QQ:2851717387
胡经理 2355265332
询单
上海一基实业有限公司 13311756052
021-60526763 13311756052 13311756131
胡经理 2355265332
询单
上海绩祥生物科技有限公司 13093077543陆经理 3985448220
询单
南通众合化工新材料有限公司 18762756250
0513-55074056
胡经理 2369399482
询单
上海腾准生物科技有限公司 19821570922
021-34053661
张经理 3003871136
询单
武汉鑫伟烨化工有限公司 18502781673
18502781673
张经理 359501377
询单
金锦乐(湖南)化学有限公司 金锦乐 1226360695
询单
赫澎(上海)生物科技有限公司 13122891558
186-16545970
张硕 3418426269
询单

2-溴-5-氯苯乙酮(935-99-9)合成路线

合成路线:1 步
反应条件:
参考文献:
Base-Catalyzed Synthesis of Substituted Indazoles under Mild, Transition-Metal-Free Conditions
Thome, Isabelle; Besson, Claire; Kleine, Tillmann; Bolm, Carsten, Angewandte Chemie, 2013, 52(29), 7509-7513
合成路线:1 步
反应条件:
参考文献:
Asymmetric Synthesis and Application of Chiral Spirosilabiindanes
Chang, Xin; Ma, Pei-Long; Chen, Hong-Chao; Li, Chuan-Ying; Wang, Peng, Angewandte Chemie, 2020, 59(23), 8937-8940
合成路线:1 步
反应条件:
参考文献:
Direct synthesis of 1-naphthylamines enabled by 6-endo-dig cyclization strategy using copper catalysis
Ma, Peng ; Wang, Jianhui ; Liu, Guiyan, Applied Organometallic Chemistry, 2022, 36(6),
合成路线:1 步
反应条件:
参考文献:
One-Pot Asymmetric Synthesis of Alkylidene 1-Alkylindan-1-ols Using Bronsted Acid and Palladium Catalysis
Faggyas, Reka J.; Calder, Ewen D. D.; Wilson, Claire; Sutherland, Andrew, Journal of Organic Chemistry, 2017, 82(21), 11585-11593
合成路线:1 步
反应条件:
参考文献:
Preparation of boron containing fungicides and their use in compositions and methods for the control and/or prevention of microbial infection in plants
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Synthesis of Secondary Unsaturated Lactams via an Aza-Heck Reaction
Shuler, Scott A.; Yin, Guoyin; Krause, Sarah B.; Vesper, Caroline M.; Watson, Donald A., Journal of the American Chemical Society, 2016, 138(42), 13830-13833
合成路线:1 步
反应条件:
参考文献:
Behavior of three bromochlorobenzenes in Friedel-Crafts acylation reactions
Cam-Van, N. T.; Diep, Bui K.; Buu-Hoi N. P., Tetrahedron, 1964, 20(10), 2195-9
合成路线:1 步
反应条件:
参考文献:
Palladium-Catalyzed Suzuki Coupling and NIS-Mediated Dehydrogenative Cycloetherification: A Concise Approach to 6,6-Disubstituted 6H-benzo[c]chromenes and Total Synthesis of Didehydroconicol
Shekhar, Chander; Satyanarayana, Gedu, European Journal of Organic Chemistry, 2022, 2022(18),
合成路线:1 步
反应条件:
参考文献:
Divergent Access to Benzocycles through Copper-Catalyzed Borylative Cyclizations
Yoon, Wan Seok; Han, Jung Tae; Yun, Jaesook, Advanced Synthesis & Catalysis, 2021, 363(21), 4953-4959
合成路线:1 步
反应条件:
参考文献:
The intramolecular reaction of acetophenone N-tosylhydrazone and vinyl: Bronsted acid-promoted cationic cyclization toward polysubstituted indenes
Wang, Zhixin; Li, Yang; Chen, Fan; Qian, Peng-Cheng; Cheng, Jiang, Chemical Communications (Cambridge, 2021, 57(14), 1810-1813
合成路线:1 步
反应条件:
参考文献:
Asymmetric synthesis of 1,2-dihydronaphthalene-1-ols via copper catalyzed intramolecular reductive cyclization
Acharyya, Ranjan Kumar; Kim, Soyoung; Park, Yeji; Han, Jung Tae; Yun, Jaesook, Organic Letters, 2020, 22(20), 7897-7902
合成路线:1 步
反应条件:
参考文献:
PdII-Catalyzed Oxidative Tandem aza-Wacker/Heck Cyclization for the Construction of Fused 5,6-Bicyclic N,O-Heterocycles
Ye, Chenghao; Kou, Xuezhen; Xia, Jingzhao; Yang, Guoqiang ; Kong, Li; et al, Chemistry - An Asian Journal, 2018, 13(15), 1897-1901
合成路线:1 步
反应条件:
参考文献:
Enantioselective Bromo-oxycyclization of Silanol
Xia, Zilei; Hu, Jiadong; Shen, Zhigao; Wan, Xiaolong; Yao, Qizheng; et al, Organic Letters, 2016, 18(1), 80-83
合成路线:1 步
反应条件:
参考文献:
Palladium-Catalyzed Aerobic Aminooxygenation of Alkenes for Preparation of Isoindolinones
Kou, Xuezhen; Li, Yu; Wu, Liang; Zhang, Xinghua; Yang, Guoqiang; et al, Organic Letters, 2015, 17(22), 5566-5569
合成路线:1 步
参考文献:
Synthesis of 2,3-dihydro-1H-isoindole-1-thiones via the bromine-lithium exchange between 1-bromo-2-(1-isothiocyanatoalkyl)benzenes and butyllithium
Kobayashi, Kazuhiro; Yokoi, Yuki; Nakahara, Tatsuya; Matsumoto, Naoki, Tetrahedron, 2013, 69(48), 10304-10310
合成路线:1 步
反应条件:
参考文献:
Acylated piperidine derivatives, specifically 1-(pyrrolidinylcarbonyl)piperidines, 1-(piperidinylcarbonyl)piperidines, and analogs, as melanocortin-4 receptor agonists, and their pharmaceutical compositions and therapeutic uses
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Acylated piperidine derivatives, specifically 1-[(aminocycloalkyl)carbonyl]piperidines, as melanocortin-4 receptor agonists, and their pharmaceutical compositions and therapeutic uses
, World Intellectual Property Organization, , ,
合成路线:1 步
参考文献:
Sequential One-Pot Process to Construct a Dual C-C Bond: Synthesis of Fluorenes and Total Synthesis of 4-O-Demethyl-nobilone
Shekhar, Chander; Satyanarayana, Gedu, ChemistrySelect, 2023, 8(26),