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(2-chloro-allyl)-propyl-amine | 39099-20-2

中文名称
——
中文别名
——
英文名称
(2-chloro-allyl)-propyl-amine
英文别名
2-Chlor-3-propylamino-propen;(2-Chlor-allyl)-propyl-amin;N-(2-chloroallyl)propylamine;N-(2-chloro-2-propen-1-yl)-N-propylamine;2-chloro-N-propylprop-2-en-1-amine
(2-chloro-allyl)-propyl-amine化学式
CAS
39099-20-2
化学式
C6H12ClN
mdl
MFCD12797794
分子量
133.621
InChiKey
LBTCFZQJGLOBSM-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:
    163.9±23.0 °C(Predicted)
  • 密度:
    0.936±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.8
  • 重原子数:
    8
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.666
  • 拓扑面积:
    12
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:290e70603fc57765e1c21fa36d5050dd
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反应信息

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文献信息

  • Method for the production of sulphamic acid halogenides
    申请人:Hamprecht Gerhard
    公开号:US20050159622A1
    公开(公告)日:2005-07-21
    The present invention relates to a process for preparing sulfamoyl halides of primary or secondary amines, comprising the following steps: i) reacting a primary or secondary amine Al with at least equimolar amounts of SO 3 or an SO 3 source in the presence of at least equimolar amounts of a tertiary amine A2, based in each case on the amine A1, and ii) reacting the reaction mixture obtained in step i) with at least the amount of a phosphorus halide required by the stoichiometry; The invention further relates to a process for preparing sulfonic diamides, comprising the preparation of sulfamoyl halides by means of carrying out steps i) and ii) and subsequently reacting the sulfamoyl halide obtained with ammonia. The invention further relates to the use of this process for preparing active herbicidal ingredients having a sulfuric diamide structure. The invention further relates to novel sulfamoyl chlorides.
    本发明涉及一种制备一级或二级胺的磺酰卤化物的方法,包括以下步骤:i)在至少相当摩尔量的三级胺A2的存在下,将一级或二级胺A1与SO3或SO3源至少相当摩尔量反应,基于每种情况下的胺A1,ii) 将步骤i)中获得的反应混合物与至少所需的卤化物量按化学计量反应。本发明还涉及一种制备磺酰二胺的方法,包括通过执行步骤i)和ii)制备磺酰卤化物,随后将所得的磺酰卤化物反应。本发明还涉及使用该方法制备具有磺酰二胺结构的活性除草剂成分。本发明还涉及新型磺酰氯化物。
  • Method of combating weeds
    申请人:HARRY TILLES
    公开号:US03298817A1
    公开(公告)日:1967-01-17
  • FR2250740
    申请人:——
    公开号:——
    公开(公告)日:——
  • VERFAHREN ZUR HERSTELLUNG VON SULFONSÄUREDIAMIDEN
    申请人:BASF SE
    公开号:EP1506169B1
    公开(公告)日:2009-12-23
  • AVERMECTIN B1 AND AVERMECTIN B1 MONOSACCHARIDE DERIVATIVES HAVING AN ALKOXYMETHYL SUBSTITUENT IN THE 4"-OR 4'-POSITION
    申请人:Maienfisch Peter
    公开号:US20100210574A1
    公开(公告)日:2010-08-19
    What is described are a compound of the formula wherein n is 0 or 1; A-B is —CH═CH— or —CH 2 —CH 2 —; R 1 is C 1 -C 12 -alkyl, C 3 -C 8 -cycloalkyl or C 2 -C 12 -alkenyl; R 2 is for example C 1 -C 12 -alkyl, C 2 -C 12 -alkenyl or C 2 -C 12 -alkinyl; which are optionally substituted with one to five substituents selected from the group consisting of OH, halogen, CN, —N 3 , —NO 2 , C 3 -C 8 -Cycloalkyl, norbornylenyl-, C 3 -C 8 -Cycloalkenyl; C 3 -C 8 -halocycloalkyl, C 1 -C 12 -alkoxy, C 1 -C 6 -alkoxy-C 1 -C 6 -alkoxy, C 3 -C 8 -cycloalkoxy, C 1 -C 12 -haloalkoxy, C 1 -C 12 -alkylthio, C 3 -C 8 -cycloalkylthio, C 1 -C 12 -haloalkylthio, C 1 -C 12 -alkylsulfinyl, C 3 -C 8 -cycloalkylsulfinyl, C 1 -C 12 -haloalkylsulfinyl, C 3 -C 8 -halocycloalkylsulfinyl, C 1 -C 12 -alkylsulfonyl, C 3 -C 8 -cycloalkylsulfonyl, C 1 -C 12 -haloalkylsulfonyl, C 3 -C 8 -halocycloalkylsulfonyl, —NR 4 R 6 , —X—C(═Y)—R 4 , —X—C(═Y)—Z—R 4 , —P(═O)(OC 1 -C 6 -alkyl) 2 , aryl, heterocyclyl, aryloxy, arylthio and heterocyclyloxy; R 3 is for example H, C 1 -C 12 -alkyl or C 1 -C 12 -alkyl which is optionally substituted and, where applicable, to E/Z isomers, mixtures of E/Z isomers and/or tautomers, in each case in free form or in salt form; a process for preparing and using these compounds and their tautomers; pesticides whose active compound is selected from these compounds and their tautomers; and a process for preparing these compounds and compositions, and the use of these compounds and compositions.
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