摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

Octan-3-yl formate | 84434-65-1

中文名称
——
中文别名
——
英文名称
Octan-3-yl formate
英文别名
——
Octan-3-yl formate化学式
CAS
84434-65-1
化学式
C9H18O2
mdl
MFCD06796192
分子量
158.24
InChiKey
PPJCPDSDDKESKL-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

物化性质

  • 沸点:
    195.9±9.0 °C(Predicted)
  • 密度:
    0.873±0.06 g/cm3(Predicted)
  • LogP:
    3.30
  • 物理描述:
    Colourless liquid; Minty, spicy, herb-like aroma with fruity undertones
  • 溶解度:
    Soluble in fats and oils; insoluble in water
  • 折光率:
    1.413-1.417

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    11
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.888
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    甲酸3-辛醇Iron(III) nitrate nonahydrate 、 sodium iodide 作用下, 生成 Octan-3-yl formate
    参考文献:
    名称:
    Stereodivergent Protein Engineering of Fatty Acid Photodecarboxylase for Light‐Driven Kinetic Resolution of Sec‐Alcohol Oxalates
    摘要:
    Abstract

    Stereodivergent engineering of one enzyme to create stereocomplementary variants for synthesizing optically pure molecules with tailor‐made (R) or (S) configurations on an optional basis is highly desirable and challenging. This study aimed to engineer fatty acid photodecarboxylase from Chlorella variabilis (CvFAP) using the focused rational iterative site‐specific mutagenesis (FRISM) strategy to obtain two highly stereocomplementary variants with excellent selectivity (both giving products with up to 99 % e.e.). These variants were used for the CvFAP‐catalyzed light‐driven kinetic resolution of oxalates or oxamic acids prepared from the corresponding sec‐alcohols or amines, providing a new biotransformation process for preparing chiral sec‐alcohols and amines. Molecular dynamics simulation, kinetic data and transient spectra revealed the source of selectivity. This study represents the first example of the kinetic resolution of sec‐alcohols or amines catalyzed by a pair of stereocomplementary CvFAPs.

    DOI:
    10.1002/anie.202318374
点击查看最新优质反应信息

文献信息

  • [EN] 3-ALKYLIDENEHYDRAZINO SUBSTITUTED HETEROARYL COMPOUNDS AS THROMBOPOIETIN RECEPTOR ACTIVATORS<br/>[FR] UTILISATION DE COMPOSES HETEROARYLES A SUBSTITUTION 3-ALKYLIDENEHYDRAZINO EN TANT QU'ACTIVATEURS DU RECEPTEUR DE LA THROMBOPOIETINE
    申请人:NISSAN CHEMICAL IND LTD
    公开号:WO2004108683A1
    公开(公告)日:2004-12-16
    A compound represented by the formula (1): wherein A is a nitrogen atom or CR4, B is an oxygen atom, a sulfur atom or NR9 (provided that when A is a nitrogen atom, B is not NH), R1 is a C2-14; aryl group, L1 is a bond, CR10R11, an oxygen atom, a sulfur atom or NR12, X is OR13, SR13 or NR14NR15, R2 is a hydrogen atom, a formyl group, a C1-10; alkyl group or the like, L2 is a bond or the like, L3 is a bond, CR17R18, an oxygen atom, a sulfur atom or NR19, L4 is a bond, CR20R21, an oxygen atom, a sulfur atom or NR22, Y is an oxygen atom, a sulfur atom or NR23, and R3 is a C2-14; aryl group, a tautomer, prodrug or pharmaceutically acceptable salt of the compound or a solvate thereof.
    化合物的结构式(1)如下:其中A是氮原子或CR4,B是氧原子、原子或NR9(但当A是氮原子时,B不是NH),R1是C2-14芳基,L1是键,CR10R11、氧原子、原子或NR12,X是OR13、SR13或NR14NR15,R2是氢原子、甲酰基、C1-10烷基或类似物,L2是键或类似物,L3是键,CR17R18、氧原子、原子或NR19,L4是键,CR20R21、氧原子、原子或NR22,Y是氧原子、原子或NR23,R3是C2-14芳基、化合物的互变异构体、前药或药学上可接受的盐或其溶剂化合物。
  • ALPHA-SUBSTITUTED VINYLTIN COMPOUND
    申请人:Tatsuta Kuniaki
    公开号:US20090023939A1
    公开(公告)日:2009-01-22
    To provide α-substituted vinyltin useful for the search for function-developing substances such as pharmaceuticals/agrichemicals and functional materials and for the construction of a compound library. An α-substituted vinyltin compound represented by the formula (1), a tautomer or salt of the compound or a solvate thereof: R 2 CH═C(R 3 )Sn(R 1 ) 3 (1) wherein R 1 is a C 1-10 alkyl group, a C 2-14 aryl group or the like, R 2 is a C 2-14 aryl group, a C 2-9 heterocyclyl group, a C 3-10 cycloalkyl group or the like, and R 3 is a carbamoyl group, a thiocarbamoyl group, an isocyanate group, an isothiocyanate group, a formylamino group, a thioformylamino group, an isonitrile group, an urea group, a carbamate group or the like.
    提供α-取代的乙烯基,用于寻找功能发展物质,如药物/农药和功能材料,以及用于构建化合物库。由下式表示的α-取代的乙烯基化合物(1)或其互变异构体或盐或溶剂合物:R2CH═C(R3)Sn(R1)3(1)其中R1是C1-10烷基,C2-14芳基或类似物,R2是C2-14芳基,C2-9杂环基,C3-10环烷基或类似物,R3是基甲酰基,基甲酰基,异氰酸酯基,异硫氰酸酯基,甲酰基基,代甲酰基基,异腈基,基,氨基甲酸酯基或类似物。
  • [EN] ENOL ETHER PROPERFUME<br/>[FR] PRO-PARFUM D'ÉNOLÉTHER
    申请人:FIRMENICH & CIE
    公开号:WO2019243501A1
    公开(公告)日:2019-12-26
    The present invention relates to compounds of formula (I) as properfume compounds. In particular, the present invention relates to a method to release a compound being a ketone or aldehyde of formula (II), a formate ester of formula (III) and/or an alcohol of formula (IV) by exposing the compound of formula (I) to an environment wherein it is oxidized. Moreover, the present invention relates to a perfuming composition and a perfume consumer product comprising at least one compound of formula (I).
    本发明涉及化合物的结构式(I)作为香料化合物。具体而言,本发明涉及一种释放结构式(I)化合物的方法,其中该化合物是结构式(II)的酮或醛、结构式(III)的甲酸酯和/或结构式(IV)的醇,通过将结构式(I)的化合物暴露在氧化环境中。此外,本发明涉及一种香组合物和一种香消费产品,其中包括至少一种结构式(I)的化合物。
  • [EN] PRO-PERFUME COMPOSITIONS<br/>[FR] COMPOSITIONS DE PROPARFUM
    申请人:FIRMENICH & CIE
    公开号:WO2021123144A1
    公开(公告)日:2021-06-24
    The present invention relates to a perfuming composition comprising at least two properfume compounds selected from the group consisting of a pro-perfume compound releasing a perfume compound upon exposure to light, a pro-perfume compound releasing a perfume compound upon exposure to air/oxygen, a pro-perfume compound releasing a perfume compound upon exposure to heat, a pro-perfume compound releasing a perfume compound upon exposure to moisture and a pro-perfume compound releasing a perfume compound upon exposure to enzymes. The present invention further concerns a perfumed consumer product comprising the inventive perfuming composition, as well as the use of the inventive perfuming composition for improving, enhancing, conferring and/or modifying the fragrance impression and/or fragrance intensity of a consumer product.
    本发明涉及一种香组合物,包括至少两种从以下组成的适当香气化合物中选择的香气化合物:一种在光照下释放香化合物的前香化合物,一种在空气/氧气暴露下释放香化合物的前香化合物,一种在热暴露下释放香化合物的前香化合物,一种在湿气暴露下释放香化合物的前香化合物以及一种在酶暴露下释放香化合物的前香化合物。本发明进一步涉及一种含有创新香组合物的香消费产品,以及使用创新香组合物来改善、增强、赋予和/或修改消费产品的香气印象和/或香气强度。
  • [EN] ALKYL ENOL ETHER PROPERFUME<br/>[FR] PRO-PARFUM D'ALKYLÉNOLÉTHER
    申请人:FIRMENICH & CIE
    公开号:WO2020127708A1
    公开(公告)日:2020-06-25
    The present invention relates to compounds of formula (I) as properfume compounds. In particular, the present invention relates to a method to release a compound being a ketone of formula (II), a formate ester of formula (III) and/or an alcohol of formula (IV) by exposing the compound of formula (I) to an environment wherein it is oxidized. Moreover, the present invention relates to a perfuming composition and a perfumed consumer product comprising at least one compound of formula (I).
    本发明涉及化合物的公式(I),作为合适的香料化合物。具体而言,本发明涉及一种方法,通过将公式(I)的化合物暴露于氧化环境中,释放出公式(II)的酮类化合物、公式(III)的甲酸酯类化合物和/或公式(IV)的醇类化合物。此外,本发明涉及一种调香组合物和一种含有至少一种公式(I)化合物的香消费产品。
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[[[(1R,2R)-2-[[[3,5-双(叔丁基)-2-羟基苯基]亚甲基]氨基]环己基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,4R)-Boc-4-环己基-吡咯烷-2-羧酸 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-N,3,3-三甲基-N-(苯甲基)丁酰胺 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S)-2-氨基-3,3-二甲基-N-2-吡啶基丁酰胺 (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,5R,6R)-5-(1-乙基丙氧基)-7-氧杂双环[4.1.0]庚-3-烯-3-羧酸乙基酯 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素(1-6) 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸