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N,N-二乙基辛酰胺 | 996-97-4

中文名称
N,N-二乙基辛酰胺
中文别名
二乙基辛酰胺
英文名称
N,N-diethyloctanamide
英文别名
Caprylsaeure diethylamid;N,N-caprylic acid diethylamide
N,N-二乙基辛酰胺化学式
CAS
996-97-4
化学式
C12H25NO
mdl
——
分子量
199.337
InChiKey
FHJRFIYKPIXQNQ-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:
    148 °C(Press: 15 Torr)
  • 密度:
    0.8722 g/cm3
  • LogP:
    3.823 (est)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    14
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2924199090

SDS

SDS:e2d08e60b8e68259e43ee3e952485a03
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制备方法与用途

制备方法:使用表面活性剂和有机合成溶剂,这些成分广泛应用于医药、兽药、农药以及化妆品领域。

用途简介:目前暂无具体用途说明。

反应信息

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文献信息

  • Niobium Pentachloride Promoted Conversion of Carboxylic Acids to Carboxamides­: Synthesis of the 4-Aryl-1,2,3,4-tetrahydroisoquinoline Alkaloid­ Structures
    作者:Claudio C. Lopes、Rosangela S. Lopes、Marcelo S. Nery、Renata P. Ribeiro
    DOI:10.1055/s-2003-36823
    日期:——
    A practical method for the conversion of carboxylic acids to the corresponding carboxamides mediated by niobium pentachloride under mild conditions is described. The synthesis of the 4-aryl-1,2,3,4-tetrahydroisoquinoline alkaloid structures was accomplished via benzylic lithiation of N-methyl-3,4-dimethoxy-2-(4'-methoxybenzyl)benzamide.
    描述了一种在温和条件下由五氯化铌介导的将羧酸转化为相应羧酰胺的实用方法。4-aryl-1,2,3,4-四氢异喹啉生物碱结构的合成是通过 N-methyl-3,4-dimethoxy-2-(4'-methoxybenzyl)benzamide 的苄基化完成的。
  • ALPHA-AMINO ACID DERIVATIVES FOR IMPROVING SOLUBILITY
    申请人:Rudolph Thomas
    公开号:US20110039924A1
    公开(公告)日:2011-02-17
    The invention relates to the use of α-amino acid derivatives for improving the solubility of poorly soluble substances in water or aqueous solutions and to mixtures and preferred preparations.
    这项发明涉及使用α-氨基酸生物来提高溶液中难溶物质的溶解度,以及混合物和优选制剂。
  • DIGLYCOLAMIDE DERIVATIVES FOR SEPARATION AND RECOVERY OF RARE EARTH ELEMENTS FROM AQUEOUS SOLUTIONS
    申请人:UT-Battelle, LLC
    公开号:US20220002229A1
    公开(公告)日:2022-01-06
    Rare earth extractant compounds having the following structure: wherein R 1 , R 2 , R 3 , and R 4 are independently selected from alkyl groups containing 1-30 carbon atoms and optionally containing an ether or thioether linkage connecting between carbon atoms, provided that the total carbon atoms in R 1 , R 2 , R 3 , and R 4 is at least 12; R 5 and R 6 are independently selected from hydrogen atom and alkyl groups containing 1-3 carbon atoms; and provided that at least one of the conditions (i)-(iv) apply as follows: presence of a distal branched group in at least one of R 1 -R 4 (condition i), asymmetry in R 1 -R 4 (condition ii), presence of amine-containing ring (condition iii), or presence of lactam ring (condition iv). Also described are hydrophobic water-insoluble solutions containing at least one extractant compound of Formula (1), as well as method for extracting rare earth elements from aqueous solution by contacting the aqueous solution with the water-insoluble solution.
    具有以下结构的稀土萃取剂化合物:其中R1、R2、R3和R4分别从含有1-30个碳原子的烷基基团中独立选择,并且可选地包含连接碳原子之间的醚或醚连接,前提是R1、R2、R3和R4中的总碳原子至少为12;R5和R6分别从氢原子和含有1-3个碳原子的烷基基团中独立选择;并且至少应用以下条件中的一种(i)-(iv):至少在R1-R4中的一个中存在远端支链基团(条件i),R1-R4中的不对称性(条件ii),存在胺基环(条件iii),或存在内酰胺环(条件iv)。还描述了包含至少一种Formula(1)的萃取剂化合物的疏不溶性溶液,以及通过将不溶性溶液与溶液接触来从溶液中萃取稀土元素的方法。
  • Chromone complexes
    申请人:Carola Christophe
    公开号:US20070191305A1
    公开(公告)日:2007-08-16
    The invention relates to complexes of certain chromone derivatives, to compositions which comprise such derivatives, to corresponding processes for the preparation of the chromone derivatives or of compositions comprising same, and to the use thereof, in particular for the care, maintenance or improvement of the general state of the skin or hair.
    该发明涉及某些咖啡因生物的络合物,以及包含这些衍生物的组合物,以及用于制备咖啡因生物或包含它们的组合物的相应过程,并且用途包括特别用于护理、维护或改善皮肤或头发的整体状态。
  • Intermolecular sp 3 C–H bond functionalization of alkyl amides as a new method for the one-pot synthesis of functional neo alkyl amides with remote functional groups
    作者:Irena S. Akhrem、Dzhul’etta V. Avetisyan、Lyudmila V. Afanas’eva、Oleg I. Artyushin、Nikolai D. Kagramanov
    DOI:10.1016/j.tetlet.2014.11.115
    日期:2015.1
    The one-pot, regioselective, remote functionalization of amides of octanoic acid [R2NCOC7H15, NR2 = NH2, NEt2, NC4H8O, (morpholinyl)] via Csp3–H bond cleavage with CO and various nucleophiles (EtOH, iPrOH, CF3CH2OH, H(CF2)2CH2OH, C8H17SH, Et2NH, morpholine, furan, thiophene, and anisole) in the presence of the superelectrophilic complex, CBr4·2AlBr3 has been performed for the first time. This methodology
    通过CO裂解Csp 3 -H键,对辛酸[R 2 NCOC 7 H 15,NR 2  = NH 2,NEt 2,NC 4 H 8 O,(吗啉基)]的酰胺进行一锅区域选择性远程官能化。在超亲电子存在下,以及各种亲核试剂(EtOH,i PrOH,CF 3 CH 2 OH,H(CF 2)2 CH 2 OH,C 8 H 17 SH,Et 2 NH,吗啉,呋喃噻吩苯甲醚)配合物,CBr 4 ·2AlBr第一次执行3。这种方法提供了具有新结构的远程官能团的酰胺的新的具有合成挑战性和有希望的衍生物的获取。已证明使用CBr 4 ·2AlBr 3将辛烷酰胺氧化环化为具有C(Me)Et基团且与杂原子相邻的六元环酰胺。
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