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amyl methyl sulfoxide | 1561-74-6

中文名称
——
中文别名
——
英文名称
amyl methyl sulfoxide
英文别名
1-methanesulfinyl-pentane;Methyl-amyl-sulfoxid;1-methylsulfinylpentane
amyl methyl sulfoxide化学式
CAS
1561-74-6
化学式
C6H14OS
mdl
——
分子量
134.243
InChiKey
ULWIIGXPNIHTMQ-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:
    243.9±9.0 °C(Predicted)
  • 密度:
    0.979±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    8
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    36.3
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    amyl methyl sulfoxideS-1,1'-联-2-萘酚 以2%的产率得到
    参考文献:
    名称:
    TODA, FUMIO;MORI, KOJI;SATO, ATSUSHI, BULL. CHEM. SOC. JAP., 61,(1988) N1, C. 4167-4169
    摘要:
    DOI:
  • 作为产物:
    描述:
    戊基甲基硫 在 tetrabutylammonium tetrafluoroborate 、 氧气 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以62%的产率得到amyl methyl sulfoxide
    参考文献:
    名称:
    硫化物与分子氧或水的电化学氧化:亚砜和砜的可转换制备
    摘要:
    开发了一种实用且环保的电化学催化硫化物可控好氧氧化方法。亚砜和砜的可切换制备可通过反应时间有效控制,其中分子氧和水均可在催化剂和无外部氧化剂条件下作为氧源。该电化学方案具有广泛的底物范围和优异的位点选择性,已成功应用于一些含硫药物及其衍生物的改性。
    DOI:
    10.1039/d1ob01756j
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文献信息

  • [EN] A PROCESS FOR PREPARING INTERMEDIATES OF 10-PROPARGYL-10-DEAZAAMINOPTERIN (PRALATREXATE) SYNTHESIS AND THE INTERMEDIATES THEREOF<br/>[FR] PROCÉDÉ POUR LA PRÉPARATION D'INTERMÉDIAIRES DE SYNTHÈSE DE 10-PROPARGYL-10-DÉAZAAMINOPTÉRINE (PRALATREXATE) ET SES INTERMÉDIAIRES
    申请人:AVRA LAB PRIVATE LTD
    公开号:WO2013164856A1
    公开(公告)日:2013-11-07
    A process for preparation of 4-(1-(2,4-diaminopteridin-6-yl)pent-4-yn-2-yl)benzoic acid and other key intermediates in synthesis of 10-propargyl-10-deazaaminopterin (Pralatrexate) and the intermediates thereof. The 10-propargyl-10-deazaaminopterin (Pralatrexate) is obtained by peptide formation and ester hydrolysis of the intermediate compound 4-(1-(2,4-diaminopteridin-6-yl)pent-4-yn-2-yl)benzoic acid by methods known in the art.
    制备10-丙炔基-10-去氨基甲葉酸(Pralatrexate)及其关键中间体4-(1-(2,4-二氨基喹啉-6-基)戊-4-炔基-2-基)苯甲酸的方法,以及合成中间体的其他关键中间体的过程。通过已知的方法,通过中间体化合物4-(1-(2,4-二氨基喹啉-6-基)戊-4-炔基-2-基)苯甲酸的肽形成和酯水解获得10-丙炔基-10-去氨基甲葉酸(Pralatrexate)。
  • HALOALKYLSULFONANILIDE DERIVATIVE
    申请人:Kai Masanori
    公开号:US20120029187A1
    公开(公告)日:2012-02-02
    Novel herbicides are provided. A haloalkylsulfonanilide derivative represented by the formula (1) or an agrochemically acceptable salt thereof: the formula (1): wherein Z is —C(R 9 )(R 10 )— or —N(R 11 )—, A is an oxygen atom, a sulfur atom or —N(R 12 )—, W is an oxygen atom or a sulfur atom, m is an integer of from 0 to 3, n is an integer of from 0 to 3, m+n is from 1 to 3, R 1 is halo C 1 -C 6 alkyl, R 2 is a hydrogen atom, C 1 -C 6 alkyl or the like, each of R 3 and R 4 is independently a hydrogen atom, C 1 -C 6 alkyl or the like, each of R 5 , R 6 , R 7 , R 8 , R 9 and R 10 is independently a hydrogen atom, a halogen, C 1 -C 6 alkyl or the like, each of R 11 and R 12 is a hydrogen atom, C 1 -C 6 alkyl, halo C 1 -C 6 alkyl or the like, and X is independently a hydrogen atom, a halogen, C 1 -C 6 alkyl, or the like.
    提供新型除草剂。 一种由式(1)表示的卤烷基磺酰苯胺衍生物或其农药可接受的盐: 式(1): 其中Z为—C(R9)(R10)—或—N(R11)—,A为氧原子、硫原子或—N(R12)—,W为氧原子或硫原子,m为0至3的整数,n为0至3的整数,m+n为1至3,R1为卤代C1-C6烷基,R2为氢原子、C1-C6烷基或类似物,R3和R4中的每一个独立地为氢原子、C1-C6烷基或类似物,R5、R6、R7、R8、R9和R10中的每一个独立地为氢原子、卤素、C1-C6烷基或类似物,R11和R12中的每一个为氢原子、C1-C6烷基、卤代C1-C6烷基或类似物,X独立地为氢原子、卤素、C1-C6烷基或类似物。
  • PYRAZOLE-3-CARBOXYLIC ACID AMIDE DERIVATIVE AND PEST CONTROL AGENT
    申请人:KUMIAI CHEMICAL INDUSTRY CO., LTD.
    公开号:US20200199096A1
    公开(公告)日:2020-06-25
    Embodiments provide a harmful organism control agent containing a pyrazole-3-carboxylic acid amide derivative or a salt thereof as an active ingredient, having an excellent harmful organism controlling effect. A pyrazole-3-carboxylic acid amide derivative represented by general formula [I]: (wherein, R 1 , R 2 , R 3 , R 4 , and R 5 represent a hydrogen atom, halogen atom, C 1 -C 6 alkyl group or the like, R 6 represents a C 1 -C 12 alkyl group, C 1 -C 12 haloalkyl group or the like, R 7 and R 8 represent a hydrogen atom, C 1 -C 12 alkyl group or the like) or an agriculturally acceptable salt thereof, and a harmful organism control agent containing the pyrazole-3-carboxylic acid amide derivative or an agriculturally acceptable salt thereof as an active ingredient.
    实施例提供了一种含有吡唑-3-羧酸酰胺衍生物或其盐作为活性成分的有害生物控制剂,具有出色的有害生物控制效果。一种由通式[I]表示的吡唑-3-羧酸酰胺衍生物:(其中,R1、R2、R3、R4和R5代表氢原子、卤原子、C1-C6烷基或类似物,R6代表C1-C12烷基、C1-C12卤代烷基或类似物,R7和R8代表氢原子、C1-C12烷基或类似物)或其农业可接受的盐,以及一种含有吡唑-3-羧酸酰胺衍生物或其农业可接受的盐作为活性成分的有害生物控制剂。
  • Method for Producing Aldehyde and Ketone
    申请人:Yamashita Miyoshi
    公开号:US20110282102A1
    公开(公告)日:2011-11-17
    Provided is a highly efficient method for the production of aldehydes and ketones, which is inexpensive, exhibits high reactivity, and is capable of easy separation of byproduct after the reaction. More particularly, there is provided a method for producing an aldehyde or a ketone, comprising at least an oxidation step of oxidizing a primary alcohol or a secondary alcohol in the presence of a polymeric carbodiimide represented by the following formula (1) and having a weight-average molecular weight of 300 to 5000, and a sulfoxide compound, together with an acid and a base, or together with a salt of the acid and the base.
    提供了一种高效的生产醛和酮的方法,该方法廉价、具有高反应性,并能够在反应后轻松分离副产物。更具体地,提供了一种生产醛或酮的方法,包括至少一个氧化步骤,即在聚合物碳二亚胺(表示为以下式(1)且具有分子量为300至5000的重均分子量)和亚砜化合物的存在下氧化一级醇或二级醇,以及酸和碱,或者酸和碱的盐。
  • [EN] N-THIO-ANTHRANILAMIDE COMPOUNDS AND THEIR USE AS PESTICIDES<br/>[FR] COMPOSÉS N-THIO-ANTHRANILAMIDES ET LEUR UTILISATION COMME PESTICIDES
    申请人:BASF SE
    公开号:WO2013024009A1
    公开(公告)日:2013-02-21
    The present invention relates to N-thio-anthranilamide compounds of the formula (I), the stereoisomers, the salts, the tautomers and the N-oxides thereof, wherein R1 is halogen or halomethyl; R2 is hydrogen, halogen or cyano; R3 is hydrogen, C1-C4 alkyl, C1-C4 haloalkyl, C2-C6-alkenyl or the like; R4 is halogen; R5 and R6 independently of each other are optionally substituted C1-C6-alkyl, C3-C6-cycloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, phenyl, or together represent an (hetero)aliphatic chain, or the like; k is 0 or 1. The present invention further relates to a method for combating or controlling invertebrate pests, to a method for protecting plant propagation material and/or the plants which grow therefrom, to plant propagation material comprising at least one compound according to the present invention, to a method for treating or protecting an animal from infestation or infection by parasites, to a process for the preparation of a composition for treating infested or infected animals and/or for protecting animals against infestation or infection by parasites, and to a compound according to the invention for use as a medicament.
    本发明涉及公式(I)的N-硫代苯甲酰胺化合物,其立体异构体,盐,互变异构体和N-氧化物,其中R1是卤素或卤代甲基;R2是氢,卤素或氰基;R3是氢,C1-C4烷基,C1-C4卤代烷基,C2-C6-烯基或类似物;R4是卤素;R5和R6彼此独立地是可选择取代的C1-C6烷基,C3-C6环烷基,C2-C6烯基,C2-C6炔基,苯基,或者一起代表一个(杂)脂肪链,或类似物;k为0或1。本发明还涉及用于对抗或控制无脊椎动物害虫的方法,用于保护植物繁殖材料和/或由此生长的植物的方法,包括至少一种根据本发明的化合物的植物繁殖材料,用于治疗或保护动物免受寄生虫侵扰或感染的方法,用于制备用于治疗受感染动物和/或保护动物免受寄生虫侵扰或感染的组合物的方法,以及用于作为药物的本发明的化合物。
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