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N,N-二甲基-2,2-二甲基乙烷次磺酰胺 | 64037-64-5

中文名称
N,N-二甲基-2,2-二甲基乙烷次磺酰胺
中文别名
——
英文名称
N,N-dimethyl t-butylsulfenamide
英文别名
(tert-butylthio)dimethylamine;2-methyl-propane-2-sulfenic acid dimethylamide;2-Methyl-propan-2-sulfensaeure-dimethylamid;N.N-Dimethyl-S-tert.-butyl-thiohydroxylamin;tert-butylthio-dimethyl-amine;N,N-Dimethyl-tert-butylsulfenamide;N-tert-butylsulfanyl-N-methylmethanamine
N,N-二甲基-2,2-二甲基乙烷次磺酰胺化学式
CAS
64037-64-5
化学式
C6H15NS
mdl
——
分子量
133.258
InChiKey
GRHWFPGYJYPMEQ-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):
    1.7
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    28.5
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2930909090

SDS

SDS:b7ec6ee43b7dc7715a8f93b9e905aa3f
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反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Gas-phase thermolysis oft-butylsulfenamides:N, N-dimethylt-butylsulfenamide, 2,6-dimethylpiperidinylt-butylsulfenamide, andN-t-butylt-butylsulfenamide
    摘要:
    The amide derivatives of t-butylsulfenic acid mentioned in the title have been thermolyzed in a stirred-flow reactor at temperatures of 273-390 degrees C and pressures of 7- 15 torr, using toluene as carrier gas, at residence times of 0.4-2 s. Isobutene formed in 95-99% yields, through order one reactions, following the Arrhenius equations: N,N-dimethyl t-butylsulfenamide:k(s(-1)) = 10(14.45+/-0.46) exp(-175 +/- 5 kj/molRT)2,6-dimethylpiperidyl t-butylsulfenamide:k(s(-1)) = 10(14.38+/-0.26) exp(-161 +/- 3 kj/molRT)N-t-butyl t-butylsulfenamide:k(s(-1)) = 10(14.75+/-0.37) exp(-184 +/- 7 kj/molRT)These thermolyses are considered to take place through unimolecular, four-center cyclic transition-state reaction mechanisms, giving rise to isobutene plus the corresponding S-unsubstituted thiohydroxylamines. The latter decompose outside the reactor at temperatures above -78 degrees C forming free sulfur and dimethylamine. 2,6-dimethylpiperidine, and t-butylamine, respectively. (C) 1996 John Wiley & Sons, Inc.
    DOI:
    10.1002/(sici)1097-4601(1996)28:5<353::aid-kin4>3.0.co;2-u
  • 作为产物:
    参考文献:
    名称:
    Peyron; Laplaine, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1948, vol. 227, p. 132
    摘要:
    DOI:
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文献信息

  • Rheinboldt; Mott, Chemische Berichte, 1939, vol. 72, p. 668
    作者:Rheinboldt、Mott
    DOI:——
    日期:——
  • OXADIAZOLINE COMPOUND OR SALTS THEREOF, AGRICULTURAL AND HORTICULTURAL BACTERICIDE CONTAINING SAID COMPOUND, AND METHOD FOR USING SAME
    申请人:NIHON NOHYAKU CO., LTD.
    公开号:US20220386614A1
    公开(公告)日:2022-12-08
    In production of crops of agriculture and horticulture or the like, damage caused by diseases is still large, and, due to factors such as occurrence of resistant diseases to existing drugs, development of new agrohorticultural fungicides is desired. General formula (I) As a result of intensive research to develop novel fungicides, the present inventors found that the compound represented by the general formula (I) of the present invention or a salt thereof is useful as an agrohorticultural fungicide to complete the present invention.
  • US7342016B2
    申请人:——
    公开号:US7342016B2
    公开(公告)日:2008-03-11
  • US9745321B2
    申请人:——
    公开号:US9745321B2
    公开(公告)日:2017-08-29
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同类化合物

甲磺酸 N,N-二甲基-2,2-二甲基乙烷次磺酰胺 2-甲基异噻唑烷 2-氰基-2-五氟苯基丁酸乙酯 N-methyl-N-tert.-octylthiomethylamine hydrochloride N-methyl-N-ethylthiomethylamine hydrochloride N-methyl-N-isopropylthiomethylamine hydrochloride perfluoro-2-methyl-1-cyclopenten-N,N-diethylsulfenamide 2-β-hydroxyethylthioethylamine hydrochloride 2-Amino-aethan-1-sulfensaeure N,N'-bis(1,1,1,2,3,3,3-heptafluoropropan-2-ylsulfanyl)-N,N'-dimethylethane-1,2-diamine N-[(1,1,2,2-Tetrachloroethyl)sulfanyl]methanamine 2-methyl-3,6-dihydro-1,2-thiazine N,N-dibutyl-hexane-1-sulfenamide N-[2-(dimethylaminosulfanyl)ethylsulfanyl]-N-methylmethanamine N-(butylthio)-tert-butylamine 1,1-dimethyl-ethanesulfenic acid dibutylamide N-Methylmethansulfenamid N-(tert-butylthio)ethylamine N-(tert-butylthio)butylamine N-(tert-butylthio)cyclohexylamine N,N-Dimethyl-2-chlortetrafluoraethansulfenamid N-<2-(Methlthio)-ethylthio>-dimethylamin N,N-Di-n-butylmethansulphenamid nonafluoro-n-butanesulfenic acid N-(Chlormethylthio)diethylamin N-[2-[2-[ethyl(methyl)amino]sulfanylethoxy]ethylsulfanyl]-N-methylethanamine N-ethyl-N-methyl-hexanesulfenamide N-(tert-butylthio)methylamine 2-isopropyl-4,5-dimethyl-3,6-dihydro-1,2-thiazine N-(Chlormethylthio)dimethylamin N-[1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-yl]sulfanyl-N-methylmethanamine N-(Propan-2-yl)-N-(propylsulfanyl)propan-2-amine N-Ethyl-N-(propylsulfanyl)ethanamine N,N-dipropyl-propane-1-sulfenamide 2-methyl-N-(2-methylpropyl)-N-propylsulfanylpropan-1-amine N-Butylpropanesulfenamide N,N-diethylmethanesulfenamide 1-Chlor-N-(1,1,3,3-tetramethylbutyl)-1,1-bis(trifluormethyl)methansulfenamid N-(1-Adamantyl)-1-chlor-1,1-bis(trifluormethyl)methansulfenamid N-(tert-butylthio)isopropylamine 4-Propyl-1,3,4-oxathiazinane (5Z)-3-(methylsulfanylamino)-5-[(Z)-prop-1-enyl]nona-1,5-dien-2-olate N-ethyl-N-ethylsulfanyl-2-(methylideneamino)ethenamine 4,4-Dichloro-3-octylidene-1,2-thiazolidine N,2-dimethyl-N-methylsulfanylpentan-1-amine (1R,2R)-1,2-bis(hydroxysulfanyl)ethane-1,2-diol 2-(Methylaminosulfanyl)ethanamine 2-Ethyl-3-hydroxysulfanylbutan-1-ol 2-ethyl-2-methyl-N-(5-methylhexyl)-N-methylsulfanylhexan-1-amine