931-23-7 (羟基丁烯内酯,Hydroxybutenolide)

CAS号:
931-23-7
中文名称:
羟基丁烯内酯
英文名称:
Hydroxybutenolide
分子式:
C5H6O3
分子量:
114.099341869354

羟基丁烯内酯(931-23-7)名称与标识符

名称

英文别名:
2(5H)-Furanone, 5-hydroxy-3-methyl-;2-hydroxy-4-methyl-2H-furan-5-one;5-Hydroxy-3-methyl-2(5H)-furanone (ACI);Crotonic acid, 4,4-dihydroxy-2-methyl-, γ-lactone (7CI);2(5H)-Furanone, 3,5-dihydroxy-;2,5-Dihydro-5-hydroxy-3-methyl-2-oxofuran;4-Hydroxy-2-methylbut-2-en-4-olide;5-Hydroxy-3-methyl-2-butenolide;5-hydroxy-3-methyl-2,5-dihydrofuran-2-one;4-Hydroxy-2-methylbut-2-enolide;DTXSID90415048;H1747;CS-0139161;C77517;931-23-7;5-hydroxy-3-methyl-2(5H)-furanone;SY219275;EN300-320927;MFCD15145822;5-hydroxy-3-methylfuran-2(5H)-one;ghl.PD_Mitscher_leg0.903;CHEBI:195253;SCHEMBL7548600;5-Hydroxy-3-methyl-2(5H)-furanone; 2,5-Dihydro-5-hydroxy-3-methyl-2-oxofuran; 4-Hydroxy-2-methylbut-2-en-4-olide; 5-Hydroxy-3-methyl-2-butenolide; 4,4-Dihydroxy-2-methyl gamma-Lactone Crotonic Acid;5-HYDROXY-3-METHYL-5H-FURAN-2-ONE;

标识符

MDL:
MFCD15145822
InChIKey:
HQIZYPQNJWENRT-UHFFFAOYSA-N
Inchi:
1S/C5H6O3/c1-3-2-4(6)8-5(3)7/h2,4,6H,1H3
SMILES:
O=C1C(C)=CC(O)O1

羟基丁烯内酯(931-23-7)物化性质

计算特性

  • 精确分子量 : 114.031694049g/mol
  • 氢键供体数量 : 1
  • 氢键受体数量 : 3
  • 可旋转化学键数量 : 0
  • 同位素质量 : 114.031694049g/mol
  • 重原子数量 : 8
  • 复杂度 : 148
  • 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 : 1
  • 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) : 0
  • 拓扑分子极性表面积 : 46.5Ų

羟基丁烯内酯(931-23-7)推荐厂家 更多厂家(19)

羟基丁烯内酯(931-23-7)合成路线

合成路线:1 步
反应条件:
参考文献:
(PCy3)2Cl2Ru:CHPh- Catalyzed Kharasch additions. Application in a formal olefin carbonylation
Lee, Belinda T.; Schrader, Thomas O.; Martin-Matute, Belen; Kauffman, Christopher R.; Zhang, Peng; et al, Tetrahedron, 2004, 60(34), 7391-7396
合成路线:1 步
反应条件:
参考文献:
A mild, efficient, and general method for the synthesis of trialkylsilyl (Z)-4-oxo-2-alkenoates and γ-hydroxybutenolides
Boukouvalas, John; Lachance, Nicolas, Synlett, 1998, (1), 31-32
合成路线:1 步
反应条件:
参考文献:
Synthesis of useful functionalized prenyl derivatives in the E or Z configuration
Solladie, Guy; Berl, Valerie, Synlett, 1991, (11), 795-6
合成路线:1 步
反应条件:
参考文献:
Structural Requirements of Strigolactones for Hyphal Branching in AM Fungi
Akiyama, Kohki; Ogasawara, Shin; Ito, Seisuke; Hayashi, Hideo, Plant and Cell Physiology, 2010, 51(7), 1104-1117
合成路线:1 步
反应条件:
参考文献:
Synthesis of Analogs of Strigolactones and Evaluation of Their Stability in Solution
Blanco-Ania, Daniel; Zwanenburg, Binne, Methods in Molecular Biology (New York, 2021, 2309, 37-55
合成路线:1 步
反应条件:
参考文献:
Methods for hydraulic enhancement of crops
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Strigolactone formulations and uses thereof
, World Intellectual Property Organization, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation and application of lactone analogs with indolin-2-one skeleton
, China, , ,
合成路线:1 步
反应条件:
参考文献:
2,5-Dimethoxy-2,5-dihydrofuran: a convenient synthon for a novel mono-protected glyoxal; synthesis of 4-hydroxybutenolides
Fell, Stephen C. M.; Harbridge, John B., Tetrahedron Letters, 1990, 31(29), 4227-8
合成路线:1 步
反应条件:
参考文献:
Preparation of thioether strigolactone derivatives and its application as plant growth regulator
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Preparation of furanyl oxime ether compounds and application thereof
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Alkenyl ether compound with strigolactone activity and application thereof for plant growth regulator
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Synthesis of highly enantio-enriched stereoisomers of hydroxy-GR24
Morris, J. C.; McErlean, C. S. P., Organic & Biomolecular Chemistry, 2016, 14(4), 1236-1238
合成路线:1 步
反应条件:
参考文献:
Friedel-Crafts reactions of aromatic derivatives with 1,4-dioxo 2,3-ethylenic compounds. IV. Reactions of 5-hydroxy- or 5-chloro-3,5-dimethyl- or -4,5-dimethyl-2(5H)-furanones
Canevet, Jean Claude; Graff, Yves, Helvetica Chimica Acta, 1979, 62(5), 1614-21
合成路线:1 步
反应条件:
参考文献:
Enantioselective Acetalization by Dynamic Kinetic Resolution for the Synthesis of γ-Alkoxybutenolides by Thiourea/Quaternary Ammonium Salt Catalysts: Application to Strigolactones
Yasui, Motohiro ; Yamada, Ayano; Tsukano, Chihiro ; Hamza, Andrea ; Papai, Imre; et al, Angewandte Chemie, 2020, 59(32), 13479-13483
合成路线:1 步
反应条件:
参考文献:
Carotenoids and related compounds. XVIII. Synthesis of cis- and cis, cis-polyenes by reactions of the Wittig type
Pattenden, Gerald; Weedon, B. C. L., Journal of the Chemical Society [Section] C: Organic, 1968, (16), 1984-97
合成路线:1 步
反应条件:
参考文献:
A new expedient synthesis of 3-methyl-2(5H)-furanone, the common substructure in strigolactones, and its proposed biosynthesis
Malik, Heetika; Rutjes, Floris P. J. T.; Zwanenburg, Binne, Synthesis, 2010, (19), 3271-3273
合成路线:1 步
反应条件:
参考文献:
Indole-3-carboxylate strigolactone analog compound capable of promoting germination of parasitic plant seed, and preparation method thereof based on indole-3-carboxylic acid
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Compound capable of bidirectionally regulating plant growth and its preparation
, China, , ,
合成路线:1 步
反应条件:
参考文献:
Novel herbicidal preparation and preparation method thereof
, China, , ,