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nicotinic acid bornyl ester | 88382-44-9

中文名称
——
中文别名
——
英文名称
nicotinic acid bornyl ester
英文别名
Nicotinsaeure-bornylester;1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl pyridine-3-carboxylate;(1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl) pyridine-3-carboxylate
nicotinic acid bornyl ester化学式
CAS
88382-44-9
化学式
C16H21NO2
mdl
MFCD24741041
分子量
259.348
InChiKey
DTFIJWHXPYDRKN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.625
  • 拓扑面积:
    39.2
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:41b1b6d4496c098945a9de0b9fc26e5c
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反应信息

  • 作为产物:
    描述:
    烟酸borneol 以2.5%的产率得到nicotinic acid bornyl ester
    参考文献:
    名称:
    Esterification reaction on deformation of mixtures of solid organic acids and alcohols under the action of pressure
    摘要:
    DOI:
    10.1007/bf00954695
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文献信息

  • Enzymatic method for producing fatty acid bornyl ester
    申请人:Jiangnan University
    公开号:US11365434B2
    公开(公告)日:2022-06-21
    The present invention provides an enzymatic method for producing a fatty acid bornyl ester including using borneol and a fatty acid as a substrate for reaction and adding a lipase in a solvent system or a solvent-free system to catalyze the esterification reaction for a period of time to obtain fatty acid bornyl ester. The present method preferably uses fatty acids or their derivatives as acyl donors to prepare fatty acid bornyl esters. By utilizing the characteristics of the substrate, the synthesis process is simple; the reaction efficiency is high; and the content of fatty acid bornyl ester is up to 97%.
    本发明提供了一种生产脂肪酸硼醇酯的酶法,包括以硼醇和脂肪酸为底物进行反应,在溶剂体系或无溶剂体系中加入脂肪酶催化酯化反应一段时间,得到脂肪酸硼醇酯。本方法优选使用脂肪酸或其衍生物作为酰基供体来制备脂肪酸硼酯。利用底物的特性,合成工艺简单,反应效率高,脂肪酸硼酯的含量可达 97%。
  • YAKOVLEVA, I. I.;ZHAROV, A. A.;ZHULIN, O. M., IZV. AN CCCP. CEP. XIM., 1983, N 9, 2174-2175
    作者:YAKOVLEVA, I. I.、ZHAROV, A. A.、ZHULIN, O. M.
    DOI:——
    日期:——
  • ENZYMATIC METHOD FOR PRODUCING FATTY ACID BORNYL ESTER
    申请人:Jiangnan University
    公开号:US20210130859A1
    公开(公告)日:2021-05-06
    The present invention provides an enzymatic method for producing a fatty acid bornyl ester including using borneol and a fatty acid as a substrate for reaction and adding a lipase in a solvent system or a solvent-free system to catalyze the esterification reaction for a period of time to obtain fatty acid bornyl ester. The present method preferably uses fatty acids or their derivatives as acyl donors to prepare fatty acid bornyl esters. By utilizing the characteristics of the substrate, the synthesis process is simple; the reaction efficiency is high; and the content of fatty acid bornyl ester is up to 97%.
  • Esterification reaction on deformation of mixtures of solid organic acids and alcohols under the action of pressure
    作者:I. I. Yakovleva、A. A. Zharov、V. M. Zhulin
    DOI:10.1007/bf00954695
    日期:1983.9
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同类化合物

(5β,6α,8α,10α,13α)-6-羟基-15-氧代黄-9(11),16-二烯-18-油酸 (3S,3aR,8aR)-3,8a-二羟基-5-异丙基-3,8-二甲基-2,3,3a,4,5,8a-六氢-1H-天青-6-酮 (2Z)-2-(羟甲基)丁-2-烯酸乙酯 (2S,4aR,6aR,7R,9S,10aS,10bR)-甲基9-(苯甲酰氧基)-2-(呋喃-3-基)-十二烷基-6a,10b-二甲基-4,10-dioxo-1H-苯并[f]异亚甲基-7-羧酸盐 (+)顺式,反式-脱落酸-d6 龙舌兰皂苷乙酯 龙脑香醇酮 龙脑烯醛 龙脑7-O-[Β-D-呋喃芹菜糖基-(1→6)]-Β-D-吡喃葡萄糖苷 龙牙楤木皂甙VII 龙吉甙元 齿孔醇 齐墩果醛 齐墩果酸苄酯 齐墩果酸甲酯 齐墩果酸乙酯 齐墩果酸3-O-alpha-L-吡喃鼠李糖基(1-3)-beta-D-吡喃木糖基(1-3)-alpha-L-吡喃鼠李糖基(1-2)-alpha-L-阿拉伯糖吡喃糖苷 齐墩果酸 beta-D-葡萄糖酯 齐墩果酸 beta-D-吡喃葡萄糖基酯 齐墩果酸 3-乙酸酯 齐墩果酸 3-O-beta-D-葡吡喃糖基 (1→2)-alpha-L-吡喃阿拉伯糖苷 齐墩果酸 齐墩果-12-烯-3b,6b-二醇 齐墩果-12-烯-3,24-二醇 齐墩果-12-烯-3,21,23-三醇,(3b,4b,21a)-(9CI) 齐墩果-12-烯-3,11-二酮 齐墩果-12-烯-2α,3β,28-三醇 齐墩果-12-烯-29-酸,3,22-二羟基-11-羰基-,g-内酯,(3b,20b,22b)- 齐墩果-12-烯-28-酸,3-[(6-脱氧-4-O-b-D-吡喃木糖基-a-L-吡喃鼠李糖基)氧代]-,(3b)-(9CI) 鼠特灵 鼠尾草酸醌 鼠尾草酸 鼠尾草酚酮 鼠尾草苦内脂 黑蚁素 黑蔓醇酯B 黑蔓醇酯A 黑蔓酮酯D 黑海常春藤皂苷A1 黑檀醇 黑果茜草萜 B 黑五味子酸 黏黴酮 黏帚霉酸 黄黄质 黄钟花醌 黄质醛 黄褐毛忍冬皂苷A 黄蝉花素 黄蝉花定