找化学品上960化工网!
960化工网

苯乙酰肼 | 937-39-3

苯乙酰肼
2-Phenylacetohydrazide
937-39-3
C8H10N2O
150.177801609039
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:苯乙酰肼结构式
70301
苯乙酰肼价格
简介
苯乙酰肼是一种化学物质,分子式是C8H10N2O。
名称和标识符
MDL MFCD00007612
InChIKey FPTCVTJCJMVIDV-UHFFFAOYSA-N
Inchi 1S/C8H10N2O/c9-10-8(11)6-7-4-2-1-3-5-7/h1-5H,6,9H2,(H,10,11)
SMILES O=C(CC1C=CC=CC=1)NN
别名信息
- 中文别名 -
  • 苯乙酰肼
  • 苯乙酸肼
  • Phenylacetic Hydrazide 苯乙酸肼
  • 苯乙酸酰肼
- 英文别名 -
  • 2-Phenylacetohydrazide
  • benzeneaceticacid,hydrazide
  • RARECHEM BG FB 0137
  • PHENYLACETIC ACID HYDRAZIDE
  • PHENYLACETHYDRAZIDE
  • 2-PHENYLACETIC ACID HYDRAZIDE
  • ASISCHEM R35457
  • Phenylacetic Hydrazide
  • 2-phenylacetohydrazide(SALTDATA: FREE)
  • SPECS AN-068
  • Benzeneacetic acid, hydrazide
  • Phenylacetylhydrazine
  • Phenylacetyl hydrazide
  • Phenacetic acid hydrazide
  • (2-Phenylacetyl)hydrazine
  • Phenylacetohydrazide
  • Phenyl-acetic acid hydrazide
  • FPTCVTJCJMVIDV-UHFFFAOYSA-N
  • Phenylacetic acid hydrazide, 98%
  • Acetic acid, phenyl-, hydrazide
  • phenyl acetic hydrazide
  • 2-phenyl-acetohydrazide
  • 2-phenylacetic h
  • Acetic acid, phenyl-, hydrazide (6CI, 7CI, 8CI)
  • 2-Phenylacetic hydrazide
  • INHd 30
  • NSC 151437
  • Phenyl acetohydrazide
  • Phenylacetic acid hydrazide
  • Phenylacetic hydrazide
物化性质
实验特性
LogP 1.31020
PSA 55.12000
折射率 1.6180 (estimate)
沸点 271.72°C (rough estimate)
熔点 115.0 to 119.0 deg-C
闪点 174.5 °C
颜色与性状 白色针状固体
溶解性 未确定
最大波长(λmax) 205(MeOH)(lit.)
密度 1.1392 (rough estimate)
计算特性
精确分子量 150.07900
氢键供体数量 2
氢键受体数量 2
可旋转化学键数量 2
同位素质量 150.079
重原子数量 11
复杂度 130
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) 0.4
互变异构体数量 2
表面电荷 0
拓扑分子极性表面积 55.1
国际标准相关数据
EINECS 151437
海关数据
海关编码 2928000090
海关数据

中国海关编码:

2928000090

概述:

2928000090 其他肼(联氨)及胲(羟胺)的有机衍生物。监管条件:无。增值税率:17.0%。退税率:9.0%。最惠国关税:6.5%。普通关税:20.0%

申报要素:

品名, 成分含量, 用途

Summary:

2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

合成路线

合成路线:1 步

反应条件:
参考文献:
New 1,3,4-oxadiazoles as an antitubercular agents
Shah, Hitesh P., Organic Chemistry: An Indian Journal, 2012, 8(12), 447-449

合成路线:1 步

反应条件:
参考文献:
Synthesis of novel 1,3,4-oxadiazole derivatives and their biological properties
Shah, Hitesh P., Organic Chemistry: An Indian Journal, 2012, 8(10), 367-369

合成路线:1 步

反应条件:
参考文献:
Synthesis of α-ketophosphonates comprising mobile hydrogens in the α position: IR, 1H, 13C, and 31P NMR spectroscopic characteristics and reactivities with primary amines and hydrazines
Hassen, Zied; Ben Akacha, Azaiez; Zantour, Hedi, Phosphorus, 2003, 178(10), 2241-2253

合成路线:1 步

反应条件:
参考文献:
Preparation of thiogalactoside derivatives for treating diabetes mellitus
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Synthesis of new S-alkylated-3-mercapto-1,2,4-triazole derivatives bearing cyclic amine moiety as potent anticancer agents
Murty, M. S. R.; Ram, Kesur R.; Rao, Rayudu Venkateswara; Yadav, J. S.; Rao, Janapala Venkateswara; et al, Letters in Drug Design & Discovery, 2012, 9(3), 276-281

合成路线:1 步

反应条件:
参考文献:
Combinatorial synthesis of 3,5-dimethylene substituted 1,2,4-triazoles
Woodard, Scott S.; Jerome, Kevin D., Combinatorial Chemistry & High Throughput Screening, 2011, 14(2), 132-137

合成路线:1 步

反应条件:
参考文献:
Crystal structures and thermochemical properties of phenyl-acetic acid furan-2-ylmethylene-hydrazide and its Ni(II) complex
Yang, Zai-wen; Ding, Zuo-cheng; Liu, Xiang-rong; Zhao, Shun-sheng; Zhang, Run-lan; et al, Wuji Huaxue Xuebao, 2015, 31(8), 1520-1528

合成路线:1 步

反应条件:
参考文献:
Method for inhibiting methionine aminopeptidase type 2 (MetAP2), and inhibitor identification methods
, World Intellectual Property Organization, , ,

合成路线:1 步

反应条件:
参考文献:
Azo type foaming agent, a manufacturing method thereof, and a resin foaming method using the same
, Korea, , ,

合成路线:1 步

反应条件:
参考文献:
Designing and exploring active N'-[(5-nitrofuran-2-yl)methylene] substituted hydrazides against three Trypanosoma cruzi strains more prevalent in Chagas disease patients
Palace-Berl, Fanny ; Pasqualoto, Kerly Fernanda Mesquita; Jorge, Salomao Doria; Zingales, Bianca; Zorzi, Rodrigo Rocha; et al, European Journal of Medicinal Chemistry, 2015, 96, 330-339

合成路线:1 步

反应条件:
参考文献:
Discovery of [1,2,4]triazole derivatives as new metallo-β-lactamase inhibitors
Yuan, Chen; Yan, Jie; Song, Chen; Yang, Fan; Li, Chao; et al, Molecules, 2020, 25(1),

合成路线:1 步

反应条件:
参考文献:
Study on DDQ-promoted synthesis of 2,5-disubstituted 1,3,4-oxadiazoles from acid hydrazides and aldehydes
Jasiak, Karolina; Kudelko, Agnieszka; Zielinski, Wojciech; Kuznik, Nikodem, ARKIVOC (Gainesville, 2017, (2), 87-106

合成路线:1 步

反应条件:
参考文献:
Intramolecular addition of acyldiazenecarboxylates onto double bonds in the synthesis of heterocycles
Prata, Jose V.; Clemente, Dina-Telma S.; Prabhakar, Sundaresan; Lobo, Ana M.; Mourato, Isabel; et al, Journal of the Chemical Society, 2002, (4), 513-528

合成路线:1 步

反应条件:
参考文献:
Development of novel liver X receptor modulators based on a 1,2,4-triazole scaffold
Goher, Shaimaa S.; Griffett, Kristine; Hegazy, Lamees; Elagawany, Mohamed; Arief, Mohamed M. H.; et al, Bioorganic & Medicinal Chemistry Letters, 2019, 29(3), 449-453

合成路线:1 步

反应条件:
参考文献:
Synthesis of monoacyl hydrazides
Rabini, Tito; Vita, Giulio, Journal of Organic Chemistry, 1965, 30(7), 2486-8

合成路线:1 步

反应条件:
参考文献:
Dynamic combinatorial chemistry to identify binders of ThiT, an S-component of the energy-coupling factor transporter for thiamin
Monjas, Leticia ; Swier, Lotteke J. Y. M.; Setyawati, Inda ; Slotboom, Dirk J.; Hirsch, Anna K. H., ChemMedChem, 2017, 12(20), 1693-1696

合成路线:1 步

反应条件:
参考文献:
Synthesis, characterization and biological properties of some newer 2-(N-substituted carboxamido methyl thio)-5-benzyl-1,3,4-oxadiazoles
Shah, Hitesh P., Organic Chemistry: An Indian Journal, 2012, 8(11), 407-409

合成路线:1 步

反应条件:
参考文献:
Preparation of thioglucosides as SGLT2 inhibitors and antidiabetics
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Synthesis of Acyl Hydrazides from Carboxamides and Hydrazine Hydrate Under Metal-Free Conditions at Room Temperature
Singh, Shweta; Kandasamy, Jeyakumar, Asian Journal of Organic Chemistry, 2023, 12(6),

合成路线:1 步

反应条件:
参考文献:
Simple and efficient strategy to synthesize PEG-aldehyde derivatives for hydrazone orthogonal chemistry
Mauri, Emanuele; Rossi, Filippo; Sacchetti, Alessandro, Polymers for Advanced Technologies, 2015, 26(12), 1456-1460
相关文献
专业数据库参考
PubChemId 70301
参考资料
Reaxys RN 775893
化合物详情(旧版)

SMILES

NNC(=O)CC1=CC=CC=C1

960化工网为您提供苯乙酰肼专业化合物百科信息,包括中文名,英文名,分子式,分子量,以及该化合物的CasNo.:937-39-3,和相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等;| WAP 版:937-39-3
平台客服 平台客服

平台在线客服