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异硫氰酰甲酸甲酯 | 35266-49-0

中文名称
异硫氰酰甲酸甲酯
中文别名
——
英文名称
methoxycarbonylisothiocyanate
英文别名
methyl isothiocyanatoformate;Methoxycarbonyl isothiocyanate;methyl N-(sulfanylidenemethylidene)carbamate
异硫氰酰甲酸甲酯化学式
CAS
35266-49-0
化学式
C3H3NO2S
mdl
——
分子量
117.128
InChiKey
LBFAAYMITJMZOC-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:
    132.5±9.0 °C(Predicted)
  • 密度:
    1.21±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    7
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    70.8
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2930909090
  • 储存条件:
    室温且干燥环境中保存。

SDS

SDS:6dd098a7e5dd3c7937c86199268d8c6c
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Jakubowitsch; Ginsburg, Zhurnal Obshchei Khimii, 1958, vol. 28, p. 1031,1034; engl. Ausg. S. 1002, 1004
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Treatment of helminth infections with substituted phenyl-thiourea
    摘要:
    苯衍生物的化学式为:- ##STR1## 其中R是1至4个碳原子的脂肪烃基,可以被卤素或烷氧基替代,R.sup.1是氢或甲基,R.sup.2是氢、卤素、烷基、烷酰氨基(可选地被3至6个碳原子的环烷基替代)、烷氧羰基氨基、烷酰基、苯甲酰基或N-甲基甲磺酰氨基,Y是一级氨基或取代氨基,具有驱虫和抗病毒活性。该化学式内的新化合物具有杀真菌作用。
    公开号:
    US04005217A1
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文献信息

  • Alkyl 4-[o-(substituted methyleneamino)-phenyl]-3-thioallophanate
    申请人:E. I. Du Pont de Nemours and Company
    公开号:US04018926A1
    公开(公告)日:1977-04-19
    Various alkyl 4-[o-(substituted methyleneamino)phenyl]3-thioallophanates are useful as fungicides and mite ovicides. The compounds are prepared by reacting alkyl 4-(o-aminophenyl)-3-thioallophanates with aldehydes or trialkyl orthoformates. Some of the compounds are prepared by further reacting the reaction product of an alkyl 4-(o-aminophenyl)-3-thioallophanate and a trialkyl orthoformate with a primary or secondary amine. Exemplary species are methyl 4-[o-(o-fluorobenzylideneamino)phenyl]-3-thioallophanate, methyl 4-[o-(4-methylbenzylideneamino)phenyl]-3-thioallophanate and methyl 4-[o-(2-furfurylideneamino)phenyl]-3-thioallophanate.
    各种烷基4-[o-(取代亚甲基氨基)苯基]3-硫代杂氮茚酸酯是有用的杀真菌剂和杀螨卵剂。这些化合物是通过将烷基4-(o-氨基苯基)-3-硫代杂氮茚酸酯与醛或三烷基原甲酸酯反应来制备的。其中一些化合物是通过将烷基4-(o-氨基苯基)-3-硫代杂氮茚酸酯和三烷基原甲酸酯的反应产物与一级或二级胺进一步反应来制备的。代表性的物种包括甲基4-[o-(o-氟苄亚胺基)苯基]-3-硫代杂氮茚酸酯,甲基4-[o-(4-甲基苄亚胺基)苯基]-3-硫代杂氮茚酸酯和甲基4-[o-(2-呋喃基甲亚胺基)苯基]-3-硫代杂氮茚酸酯。
  • Alkyl 4-[o-(substituted methyleneamino)phenyl]-3-thioallophanates
    申请人:E. I. Du Pont de Nemours and Company
    公开号:US04011213A1
    公开(公告)日:1977-03-08
    Various alkyl 4-[o-(substituted methyleneamino)phenyl] 3-thioallophanates are useful as fungicides and mite ovicides. The compounds are prepared by reacting alkyl 4-(o-aminophenyl)-3-thioallophanates with aldehydes or trialkyl orthoformates. Some of the compounds are prepared by further reacting the reaction product of an alkyl 4-(o-aminophenyl)-3-thioallophanate and a trialkyl orthoformate with a primary or secondary amine. Exemplary species are methyl 4-[o-(o-fluorobenzylideneamino)phenyl]-3-thioallophanate, methyl 4-[o-(4-methylbenzylideneamino)phenyl]-3-thioallophanate and methyl 4-[o-(2-furfurylideneamino)phenyl]-3-thioallophanate.
    各种烷基4-[o-(取代亚甲基氨基)苯基] 3-硫代亚磷酰氧基硫代磷酸盐可用作杀真菌剂和杀螨卵剂。这些化合物是通过将烷基4-(o-氨基苯基)-3-硫代亚磷酰氧基硫代磷酸盐与醛或三烷基原甲酸酯反应来制备的。其中一些化合物是通过将烷基4-(o-氨基苯基)-3-硫代亚磷酰氧基硫代磷酸盐和三烷基原甲酸酯的反应产物与一级或二级胺进一步反应来制备的。典型的物种包括甲基4-[o-(o-氟苯亚甲基氨基)苯基]-3-硫代亚磷酰氧基硫代磷酸盐、甲基4-[o-(4-甲基苯亚甲基氨基)苯基]-3-硫代亚磷酰氧基硫代磷酸盐和甲基4-[o-(2-呋喃甲基亚甲基氨基)苯基]-3-硫代亚磷酰氧基硫代磷酸盐。
  • Alkyl 4-(o-aminophenyl)-3-thioallophanates
    申请人:——
    公开号:US03950391A1
    公开(公告)日:1976-04-13
    Various alkyl 4-(o-aminophenyl)-3-thioallophanates and alkyl 4-(o-alkylaminophenyl)-3-thioallophanates are useful as fungicides and mite ovicides. The compounds are prepared by reacting an o-phenylenediamine with the appropriate alkoxycarbonylisothiocyanate and an exemplary species is methyl 4-(o-aminophenyl)-3-thioallophanate.
    各种烷基4-(邻-氨基苯基)-3-硫代亚磷酸酯和烷基4-(邻-烷基亚氨基苯基)-3-硫代亚磷酸酯可用作杀真菌剂和杀螨卵剂。这些化合物是通过将邻苯二胺与相应的烷氧羰基异硫氰酸酯反应制备的,其中一个示例是甲基4-(邻-氨基苯基)-3-硫代亚磷酸酯。
  • Substituted (alkoxycarbonylthioureido)-(acylamino)-benzene derivatives
    申请人:May and Baker Limited
    公开号:US04034107A1
    公开(公告)日:1977-07-05
    Benzene derivatives of the formula: ##STR1## wherein R.sup.1 represents alkyl, R.sup.2 represents a group --SR.sup.3, --SOR.sup.3, --SO.sub.2 R.sup.3, --OR.sup.3, --SCONH.sub.2, --SCN or --T(CH.sub.2).sub.m T.sup.1 R.sup.4 [wherein R.sup.3 represeents alkyl, cycloalkyl, alkenyl, alkynyl, aralkyl, unsubstituted or substituted aryl, or cycloalkylalkyl, R.sup.4 represents hydrogen or alkyl, T and T.sup.1 each represent oxygen, sulphur or sulphinyl, and m is an integer from 1 to 7] whose position on the benzene ring is either para to the group --NHCSNHCOOR.sup.1 or para to the group --NHCOAZ, A represents a bivalent straight-chain aliphatic hydrocarbon radical of 1 to 4 carbon atoms or a said hydrocarbon radical substituted by at least one methyl group, and Z represents a group of the formula:- ##STR2## wherein R.sup.5 represents hydrogen or alkyl, R.sup.6 represents hydrogen, alkyl or phenylalkyl, and R.sup.7 represents hydrogen or alkyl, or R.sup.6 and R.sup.7 together with the nitrogen atom to which they are attached form a 5-,6- or 7-membered heterocyclic ring optionally substituted by alkyl group(s), and X.sup.- represents a pharmaceutically acceptable anion, are new compounds useful as anthelmintics and antifungal agents.
    苯衍生物的化学式为:##STR1## 其中R.sup.1代表烷基,R.sup.2代表--SR.sup.3、--SOR.sup.3、--SO.sub.2 R.sup.3、--OR.sup.3、--SCONH.sub.2、--SCN或--T(CH.sub.2).sub.m T.sup.1 R.sup.4 [其中R.sup.3代表烷基、环烷基、烯基、炔基、芳基烷基、未取代或取代的芳基,或环烷基烷基,R.sup.4代表氢或烷基,T和T.sup.1分别代表氧、硫或亚硫基,m为1到7的整数],其位置在苯环上要么是对位于基团--NHCSNHCOOR.sup.1,要么是对位于基团--NHCOAZ,A代表1到4个碳原子的双价直链脂肪烃基或至少一个甲基基团取代的所述烃基,Z代表下式的基团:- ##STR2## 其中R.sup.5代表氢或烷基,R.sup.6代表氢、烷基或苯基烷基,R.sup.7代表氢或烷基,或R.sup.6和R.sup.7与它们连接的氮原子一起形成一个可选择地取代的5、6或7元杂环环,X.sup.-代表药用可接受的阴离子,这些新化合物可用作驱虫剂和抗真菌剂。
  • 5(6)-Benzene ring substituted benzimidazole-2-carbamate derivatives
    申请人:Syntex (U.S.A.) Inc.
    公开号:US04072696A1
    公开(公告)日:1978-02-07
    Carbalkoxythioureidobenzene derivatives represented by the following formula: ##STR1## where R is a lower alkyl group having 1 to 4 carbon atoms; R.sup.1 is --SR.sup.2, --SOR.sup.2, --SO.sub.2 R.sup.2, --OR.sup.2, --SCN, --SC(O)NR.sup.3 R.sup.4, or --M'(CH.sub.2).sub.n MR.sup.7 where n is 1-4; R.sup.2 is lower alkyl having 1 to 6 carbon atoms, cycloalkyl having 3 to 7 carbon atoms, lower alkenyl or lower alkynyl having 3 to 6 carbon atoms, aralkyl or aryl, provided that when R.sup.1 is --SO.sub.2 R.sup.2, R.sup.2 is not aralkyl or phenyl; R.sup.3 and R.sup.4 are independently hydrogen or lower alkyl having 1 to 6 carbon atoms; Y is amino, nitro, acylamino where the acyl portion has 1 to 6 carbon atoms, --NHC(O) (CH.sub.2).sub.m COOH where m is 1-6, or --NHC(S)NHCOOR; M and M' are independently O, S or ##STR2## and R.sup.7 is lower alkyl having 1 to 4 carbon atoms or aryl. The R.sup.1 substitution is either at the 4- or 5-position. The compounds are useful as pesticides, particularly as anthelmintic and antifungal agents.
    以下是该公式代表的Carbalkoxythioureidobenzene衍生物的中文翻译:其中R是具有1至4个碳原子的低碳基团;R.sup.1是--SR.sup.2,--SOR.sup.2,--SO.sub.2 R.sup.2,--OR.sup.2,--SCN,--SC(O)NR.sup.3 R.sup.4,或--M'(CH.sub.2).sub.n MR.sup.7,其中n为1-4;R.sup.2是具有1至6个碳原子的低碳基,具有3至7个碳原子的环烷基,具有3至6个碳原子的低烯基或低炔基,芳基烷基或芳基,但当R.sup.1为--SO.sub.2 R.sup.2时,R.sup.2不是芳基烷基或苯基;R.sup.3和R.sup.4独立地是氢或具有1至6个碳原子的低碳基;Y是氨基,硝基,酰胺基,其中酰基部分具有1至6个碳原子,--NHC(O) (CH.sub.2).sub.m COOH,其中m为1-6,或--NHC(S)NHCOOR;M和M'独立地是O,S或##STR2##,R.sup.7是具有1至4个碳原子的低碳基或芳基。R.sup.1取代物位于4-或5-位置。这些化合物可用作杀虫剂,特别是作为驱虫剂和抗真菌剂。
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