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N-methyl-N-trichloromethylsulphenyl-carbamoyl fluoride | 23744-46-9

中文名称
——
中文别名
——
英文名称
N-methyl-N-trichloromethylsulphenyl-carbamoyl fluoride
英文别名
N-methyl-N-trichloromethylmercaptocarbamoyl fluoride;N-methyl-N-trichloromethanesulfenylcarbamylfluoride;N-methyl-N-trichloromethanesulfenyl carbamoyl fluoride;N-methyl-N-(trichloromethylthio)carbamoyl fluoride;Methyl[(trichloromethyl)sulfanyl]carbamyl fluoride;N-methyl-N-(trichloromethylsulfanyl)carbamoyl fluoride
N-methyl-N-trichloromethylsulphenyl-carbamoyl fluoride化学式
CAS
23744-46-9
化学式
C3H3Cl3FNOS
mdl
——
分子量
226.486
InChiKey
DUJBWBJTNVLCLM-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):
    2.6
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    45.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

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文献信息

  • Heterocyclic oxime compounds and carbamoyloxime derivatives
    申请人:Union Carbide Corporation
    公开号:US04156731A1
    公开(公告)日:1979-05-29
    Heterocyclic oxime compounds are useful as intermediates in the preparation of pesticidally active carbamoyloxime compounds.
    杂环羟肟化合物在制备具有杀虫活性的羰酰羟肟化合物中作为中间体是有用的。
  • 2-(Carbamoyloximino)-4-thiazolidinone compounds as insecticidal,
    申请人:Union Carbide Corporation
    公开号:US03966953A1
    公开(公告)日:1976-06-29
    2-(carbamoyloximino)-4-thiazolidinone compounds have been found to exhibit miticidal, nematocidal or insecticidal activity.
    2-(carbamoyloximino)-4-噻唑啉酮化合物已被发现具有杀螨、杀线虫或杀虫活性。
  • Carbamate pesticidal compounds
    申请人:Union Carbide Corporation
    公开号:US04003897A1
    公开(公告)日:1977-01-18
    Novel tetrahydro thiazine carbamoyl oxime compounds having been found to exhibit exceptional insecticidal activity.
    新发现的四氢噻嗪氨基甲酰肟化合物显示出卓越的杀虫活性。
  • Combating pests with N-acylated N-methyl-carbamic acid O-pyrazol-4-yl
    申请人:Bayer Aktiengesellschaft
    公开号:US04418073A1
    公开(公告)日:1983-11-29
    N-Acylated N-methyl-carbamic acid O-pyrazol-4-yl esters of the formula ##STR1## in which R represents an optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, aralkyl or aryl radical, Z represents an acyl radical, l represents 1 or 2, m represents 1 or 2 and n represents zero or 1, which possess pesticidal activity.
    公式为##STR1##的N-酰化N-甲基-氨基甲酸O-吡唑-4-基酯,其中R代表可选择取代的烷基、烯基、炔基、环烷基、芳基或芳基基团,Z代表酰基,l代表1或2,m代表1或2,n代表零或1,具有杀虫活性。
  • Combating fungi with
    申请人:Bayer Aktiengesellschaft
    公开号:US04239766A1
    公开(公告)日:1980-12-16
    A 1-(4-phenoxy)-3,3-dimethyl-2-(N-halogenoalkylmercapto-carbamoyloxy)-1-(1,2 ,4-triazol-1-yl)-butane of the formula ##STR1## in which R.sup.1 is alkyl or optionally substituted phenyl, R.sup.2 is halogenoalkyl, X is hydrogen or halogen, Y is hydrogen or halogen, Z each independently is alkyl, cycloalkyl, alkoxy, alkylthio, halogenoalkyl, alkoxycarbonyl, optionally substituted phenyl, phenoxy or phenylalkyl, cyano or nitro, and n is 0, 1, 2, 3, 4 or 5, and physiologically acceptable acid addition salts and metal salt complexes thereof which possess fungicidal properties.
    一种具有杀真菌性能的化合物为式子##STR1##,其中R.sup.1为烷基或可选取代的苯基,R.sup.2为卤代烷基,X为氢或卤素,Y为氢或卤素,Z分别独立为烷基、环烷基、烷氧基、烷基硫基、卤代烷基、烷氧羰基、可选取代的苯基、苯氧基或苯基烷基、氰基或硝基,n为0、1、2、3、4或5,以及其生理上可接受的酸加成盐和金属盐络合物。
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