1,2-Di[N,N-Bis(2-fluoro-2,2-dinitroethyl)carbamyl]hydrozine
    21.
    发明授权
    1,2-Di[N,N-Bis(2-fluoro-2,2-dinitroethyl)carbamyl]hydrozine 失效
    1,2-二[N,N-双(2-氟-2,2-二硝基乙基)氨基甲酰基]肼

    公开(公告)号:US4414413A

    公开(公告)日:1983-11-08

    申请号:US332797

    申请日:1981-12-21

    Abstract: N,N,N',N'-tetrakis(2-fluoro-2,2-dinitroethyl) oxamide, ##STR1## which is prepared by the following reaction sequence ##STR2## N,N,N',N'-tetrakis(2-fluoro-2,2-dinitroethyl) oxamide is a high density, energetic explosive which is melt castable as well as thermally and hydrolytically stable.

    Abstract translation: N,N,N',N'-四(2-氟-2,2-二硝基乙基)草酰胺,其通过以下反应顺序制备:IMAGE>< IMAGE> N,N,N',N'-四(2-氟-2,2-二硝基乙基)草酰胺是一种高密度,高能量的爆炸物,它是可熔融浇铸的以及热和水解稳定的。

    Nitrobenzodifuroxan compounds, including their salts, and methods thereof
    23.
    发明授权
    Nitrobenzodifuroxan compounds, including their salts, and methods thereof 失效
    硝基苯并二恶唑化合物,包括它们的盐及其方法

    公开(公告)号:US07145016B1

    公开(公告)日:2006-12-05

    申请号:US10652080

    申请日:2003-08-28

    CPC classification number: C07D498/04

    Abstract: A nitrobenzodifuroxan compound having the chemical structure of: wherein two of the R1, R2, R3 and R4 comprise oxygen or are absent, and only one of R1 or R2 is present, and only one of R3 and R4 is present, and wherein x is hydrolyzed or hydrolyzable. The salt of the hydroxynitrobenzodifuroxan of this compound is useful in explosive compositions.

    Abstract translation: 具有以下化学结构的硝基苯并二呋喃糖化合物:其中R 1,R 2,R 3和R 4中的两个, SUB>包含氧或不存在,并且仅存在R 1或R 2中的一个,并且R 3和R 2中只有一个存在, 存在SUB> 4,并且其中x被水解或可水解。 该化合物的羟基硝基苯并二呋喃糖的盐可用于爆炸性组合物。

    1,3,4-oxadiazoles containing the pentafluorothio (SF.sub.5) group
    25.
    发明授权
    1,3,4-oxadiazoles containing the pentafluorothio (SF.sub.5) group 失效
    含有五氟硫基(SF5)基团的1,3,4-恶二唑

    公开(公告)号:US5292951A

    公开(公告)日:1994-03-08

    申请号:US119296

    申请日:1993-09-10

    CPC classification number: C07D271/10 C08K5/353

    Abstract: 1,3,4-Oxadiazoles of the formula ##STR1## are prepared by cyclization (dehydration) of the corresponding diacylhydines of the formula R.sub.1 C(O)NHNHC(O)R.sub.2 with phosphorous pentachloride or phosphorous oxychloride wherein R.sub.1 is --CF.sub.2 CF.sub.2 CF.sub.2 SF.sub.5, --CF.sub.2 CF.sub.2 SF.sub.5, or --CH.sub.2 SF.sub.5 and R.sub.2 is --CH.sub.2 CH.sub.2 C(NO.sub.2).sub.3, --CH.sub.2 CH.sub.2 C(NO.sub.2).sub.2 F, --CF.sub.2 CF.sub.2 CF.sub.3, --CF.sub.2 CF.sub.3, --CF.sub.3, or --CH.sub.2 SF.sub.5.

    Abstract translation: 通过使式R 1 C(O)NHNHC(O)R 2的相应的二酰基肼与五氯化磷或其氯氧化磷进行环化(脱水),其中R1是-CF2CF2CF2SF2,-CF2CF2SF5,制备式“IMAGE”的1,3,4-恶二唑 ,或-CH 2 SF 5,且R 2为-CH 2 CH 2 C(NO 2)3,-CH 2 CH 2 C(NO 2)2 F,-CF 2 CF 2 CF 3,-CF 2 CF 3,-CF 3或-CH 2 SF 5。

    High density energetic materials
    26.
    发明授权
    High density energetic materials 失效
    高密度高能材料

    公开(公告)号:US5194103A

    公开(公告)日:1993-03-16

    申请号:US695144

    申请日:1991-04-30

    CPC classification number: C06B43/00 C06B25/00 C07C381/00

    Abstract: Energetic compounds of the formula ##STR1## wherein R.sub.1 is --OCH.sub.2 CH.sub.2 C(NO.sub.2).sub.3, --OCH.sub.2 C.sub.2).sub.2 CH.sub.3, --OCH.sub.2 C(NO.sub.2).sub.3, --OCH.sub.2 CF(NO.sub.2).sub.2, --OCH.sub.2 CF.sub.2 (NO.sub.2), or --OCH.sub.2 CF.sub.3, and wherein R.sub.2 is --OCH.sub.2 CH.sub.2 C(NO.sub.2).sub.3, --OCH.sub.2 CF(NO.sub.2).sub.2, --OCH.sub.2 CF.sub.2 (NO.sub.2), --OCH.sub.2 CF.sub.3, --NH.sub.2, --NHCH.sub.2 CH.sub.2 ONO.sub.2, or --N(NO.sub.2)CH.sub.2 CH.sub.2 ONO.sub.2.

    Abstract translation: 其中R 1是-OCH 2 CH 2 C(NO 2)3,-OCH 2 C(NO 2)2 CH 3,-OCH 2 C(NO 2)3,-OCH 2 CF(NO 2)2,-OCH 2 CF 2(NO 2)或-OCH 2 CF 3的化学式 其中R2是-OCH2CH2C(NO2)3,-OCH2CF(NO2)2,-OCH2CF2(NO2),-OCH2CF3,-NH2,-NHCH2CH2ONO2或-N(NO2)CH2CH2ONO2。

    N,N'-bis(4,4,4-trinitrobutyryl)hydrazine
    27.
    发明授权
    N,N'-bis(4,4,4-trinitrobutyryl)hydrazine 失效
    N,N'-双(4,4,4-三硝基丁酰基)肼

    公开(公告)号:US5183938A

    公开(公告)日:1993-02-02

    申请号:US901620

    申请日:1992-06-15

    CPC classification number: C06B25/00 C07C243/34

    Abstract: N,N'-Bis(4,4,4-trinitrobutyryl)hydrazine which is prepared by reacting 4,-trinitrobutyryl chloride with hydrazine in methanol at low temperature. This compound is sensitive enough to be used as an initiating explosive and thermally stable enough to be used in missile warheads.

    Abstract translation: N,N'-双(4,4,4-三硝基丁酰基)肼,其通过使4,4,4-三硝基丁酰氯与肼在甲醇中在低温下反应制备。 这种化合物足够敏感,可用作起爆炸药,热稳定性足以用于导弹弹头。

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