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苯甲酸异戊酯 | 94-46-2

苯甲酸异戊酯
Isopentyl benzoate
94-46-2
C12H16O2
192.254243850708
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:苯甲酸异戊酯结构式
87563273
苯甲酸异戊酯价格
名称和标识符
MDL MFCD00026515
InChIKey MLLAPOCBLWUFAP-UHFFFAOYSA-N
Inchi 1S/C12H16O2/c1-10(2)8-9-14-12(13)11-6-4-3-5-7-11/h3-7,10H,8-9H2,1-2H3
SMILES O=C(C1C=CC=CC=1)OCCC(C)C
BRN 1946447
别名信息
- 中文别名 -
  • 苯甲酸异戊酯
  • 3,6-双(氯甲基)杜烯
  • Isoamyl Benzoate 苯甲酸异戊酯
  • 苯甲酸异戊酯 标准品
  • 异戊基苯甲酸酯
- 英文别名 -
  • Isopentyl benzoate
  • Benzoic acid isoamyl ester
  • 3-methyl-1-butanol benzoate
  • benzoic acid isopentyl ester
  • Isoamyl Benzoate
  • 3-methylbutyl benzoate
  • Isoamyl-benzoate
  • 3-methyl-1-butano benzoate
  • benzoic acid, isopentyl ester
  • Isopentyl alcohol, benzoate
  • 1-Butanol, 3-methyl-, benzoate
  • 1-(3-Methyl)butyl benzoate
  • 3-Methyl-1-butyl benzoate
  • Benzoic acid, 1-(3-methyl)butyl ester
  • Benzoic acid, 3-methylbutyl ester
  • Isoamyl benzoate (natural)
  • 1-Butanol, 3-methyl-, 1-benzoate
  • FEMA No. 2058
  • Isopentyl alcohol, benzoate (6CI,8CI)
  • 0AY72CK43K
  • benzo
  • 1-Butanol, 3-methyl-, benzoate (9CI)
  • Isopentyl alcohol, benzoate (6CI, 8CI)
  • 3-Methylbutyl benzoate
  • iso-Amyl benzoate
  • iso-Pentyl benzoate
  • Isoamyl benzoate
  • NSC 9284
  • Benzoic Acid Isoamyl Ester
  • Isopentyl Benzoate
物化性质
实验特性
LogP 2.88950
PSA 26.30000
Merck 5113
折射率 n20/D 1.494(lit.)
沸点 262°C(lit.)
闪点 >230 °F
FEMA 2058 | ISOAMYL BENZOATE
颜色与性状 无色至淡黄色液体,有果香和龙涏香香韵。
溶解性 不溶于水,能与醇、醚等多种有机溶剂混溶。对油脂和蜡的溶解能力大,能溶解松香、甘油三松香酸酯、香豆酮树脂等。对硝酸纤维素、醋酸纤维素、虫胶等的溶解能力较小。甘油醇酸树脂不溶解。
密度 0.99 g/mL at 25 °C(lit.)
计算特性
精确分子量 192.11500
氢键供体数量 0
氢键受体数量 2
可旋转化学键数量 5
同位素质量 192.11503
重原子数量 14
复杂度 169
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) 3.8
互变异构体数量
表面电荷 0
拓扑分子极性表面积 26.3
国际标准相关数据
EINECS 9284
海关数据
海关编码 2916310090
海关数据

中国海关编码:

2916310090

概述:

2916310090 其他苯甲酸及其盐和酯. 增值税率:17.0% 退税率:9.0% 监管条件:AB(入境货物通关单,出境货物通关单) 最惠国关税:6.5% 普通关税:30.0%

申报要素:

品名, 成分含量, 用途, 丙烯酸、丙烯酸盐或酯应报明包装

监管条件:

A.入境货物通关单
B.出境货物通关单

检验检疫类别:

R.进口食品卫生监督检验
S.出口食品卫生监督检验
M.进口商品检验
N.出口商品检验

Summary:

2916310090 other benzoic acid and its salts and esters。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:6.5%。general tariff:30.0%

合成路线

合成路线:1 步

反应条件:
参考文献:
Enolate-Based Regioselective Anti-Beckmann C-C Bond Cleavage of Ketones
Masek, Tomas; Jahn, Ullrich, Journal of Organic Chemistry, 2021, 86(17), 11608-11632

合成路线:1 步

参考文献:
Improved process for synthesizing isoamyl benzoate by direct esterification
Li, Xiuyu; Hua, Yuanyuan; Cao, Ming, Guangzhou Huagong, 2000, 28(4), 4-5

合成路线:1 步

反应条件:
参考文献:
Polymer-supported ytterbium perfluorooctanesulfonate [Yb(OPf)3]: A recyclable catalyst for organic reactions
Yi, Wen-Bin; Cai, Chun, Journal of Fluorine Chemistry, 2008, 129(6), 524-528

合成路线:1 步

反应条件:
参考文献:
A novel method for the synthesis of carboxylic esters catalyzed by expandable graphite
Zhang, Ying Qun; Wang, Chun; Li, Gui Shen, Chinese Chemical Letters, 2003, 14(1), 17-19

合成路线:1 步

反应条件:
参考文献:
Ionic Liquid Based Vilsmeier Reagent as a Substitute for Mitsunobu Reagent: Direct Conversion of Alcohols into Different Compounds under Ionic Liquid Conditions
Hullio, Ahmed Ali; Mastoi, G. M., International Journal of Chemistry (Toronto, 2013, 5(3), 57-69

合成路线:1 步

反应条件:
参考文献:
Hydrogenation of Alkenes via Cooperative Hydrogen Atom Transfer
Kattamuri, Padmanabha V. ; West, Julian G., Journal of the American Chemical Society, 2020, 142(45), 19316-19326

合成路线:1 步

反应条件:
参考文献:
Chemoselective protocol for O-acylation with a new catalyst
Akhlaghinia, Batool; Safaei, Elham; Larki, Paria, Trends in Organic Chemistry, 2010, 14, 93-106

合成路线:1 步

反应条件:
参考文献:
Synthesis of isoamyl benzoate catalyzed by tungstosilicic acid
Liu, Xinhe; Wang, Xueqin, Huagong Shikan, 2000, 14(6), 30-32

合成路线:1 步

反应条件:
参考文献:
Hydrogenation reduction method of tertiary alkyl alcohol in presence of zinc powder/magnesium chloride
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Radical-chain redox rearrangement of cyclic benzylidene acetals to benzoate esters in the presence of thiols
Roberts, B. P.; Smits, T. M., Tetrahedron Letters, 2001, 42(1), 137-140

合成路线:1 步

反应条件:
参考文献:
Ionic liquid based Vilsmeier reagent as an efficient reagent for esterification of alcohols and carboxylic acids
Hullio, Ahmed Ali; Mastoi, G. M.; Imran, Hassan, International Journal of Organic Chemistry, 2018, 8(1), 125-134

合成路线:1 步

反应条件:
参考文献:
Solvent-free synthesis of benzoic esters and benzyl esters in novel Bronsted acidic ionic liquids under microwave irradiation
Li, Xinzhong; Eli, Wumanjiang; Li, Gang, Catalysis Communications, 2008, 9(13), 2264-2268

合成路线:1 步

反应条件:
参考文献:
Synthesis of isoamyl benzoate catalyzed by Ti(SO4)2/SiO2
Zhang, Fu-juan; Zhang, Hong-yu; Sheng, Shu-ling; Zhang, Xiang-yu, Gongye Cuihua, 2004, 12(11), 24-26

合成路线:1 步

反应条件:
参考文献:
Preparation of isoamyl benzoate using ammonium ferric sulfate dodecahydrate as a catalyst
Yang, Xiaolin; Li, Yunshan, Huagong Shikan, 2006, 20(4), 40-41

合成路线:1 步

反应条件:
参考文献:
Esterification of fluorous biphasic system catalyzed by rare earth(III) perfluorooctanesulfonates
Yi, Wen-Bin; Cai, Chun, Youji Huaxue, 2005, 25(11), 1434-1436

合成路线:1 步

反应条件:
参考文献:
New green technology: synthesis of isoamyl benzoate catalyzed by titanium sulfate
Deng, Bin; Li, Qiangguo; Hu, Zhengshui, Baoji Wenli Xueyuan Xuebao, 2003, 23(1), 30-32

合成路线:1 步

反应条件:
参考文献:
Bis(pentafluorophenyl) disulfide as a hydrogen abstractor and an electron acceptor from the resulting radical intermediate
Tada, Masaru; Katayama, Emi; Sakurai, Naoto; Murofushi, Keita, Tetrahedron Letters, 2004, 45(1), 17-19

合成路线:1 步

反应条件:
参考文献:
Ti-Catalyzed Dehydroxylation of Tertiary Alcohols
Lin, Quan; Tong, Weiqi ; Shu, Xing-Zhong ; Chen, Yunrong, Organic Letters, 2022, 24(46), 8459-8464

合成路线:1 步

反应条件:
参考文献:
Benzoates as photosensitization catalysts and auxiliaries in efficient, practical, light-powered direct C(sp3)-H fluorinations
Yakubov, Shahboz; Stockerl, Willibald J.; Tian, Xianhai; Shahin, Ahmed; Mandigma, Mark John P.; et al, Chemical Science, 2022, 13(47), 14041-14051

合成路线:1 步

反应条件:
参考文献:
N-Benzoyl-4-dimethylaminopyridinium Chloride: A Lewis Base Adduct for Efficient Poly and Monobenzoylation
Shekunti, Ravi Kumar; Tangalipalli, Swathi; Dhonthulachitty, Chiranjeevi; Kothakapu, Sridhar Reddy; Annapurna, Padmavathi Devarakonda; et al, ChemistrySelect, 2022, 7(41),
专业数据库参考
PubChemId 87563273
参考资料
Reaxys RN 1946447
化合物详情(旧版)

SMILES

CC(C)CCOC(=O)C1=CC=CC=C1

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