CAS: 1436-59-5; Cis-Cyclohexane-1,2-Diamine

该化合物是有机化合物,其特征是环氧环,在相邻碳原子上安装了两个有矿功能的组,这种结构安排与转对口相比,导致一个较紧凑和不那么受立体阻塞的分子.该化合物一般没有色素,可粉黄黄色液体或固态,取决于温度和纯度.该化合物由于矿体组的存在而具有基本特性,允许其参与各种化学反应,包括核循环替代和与金属离子的协调.Cis-1-2-Cyclohexanediami在水和极地有机溶剂中溶解,使其在各种应用中有用,包括作为有机合成的建筑块,聚合物的生产,以及协调化学中的结晶体化学.其独特的立体化学学能够影响其构成的化合物的再活性和特性,从而在工业和研究环境中都引起兴趣.在处理该化合物时,应当采取安全防范措施,因为它可能会对皮肤和眼睛产生刺激.

结构式图片

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REACH注册ECHA物质C&L通报REACH预注册

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CAS号317595-54-3 (2-氨基环己基)氨基甲酸叔丁酯 | CAS号36818-07-2 3-氧代-3,4-二氢-2-喹... | CAS号365996-30-1 (1S,2R)-N1-(叔丁氧... | CAS号2562-37-0 1-硝基环己烯 | CAS号184954-75-4 顺-N1-叔丁氧羰基-1,2-环己二胺 | CAS号90605-88-2 1,2-Cyclohexane...

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    专利号:US-8735586-B2
    优先权日:2007-06-26
    标 题 :Regioselective copper catalyzed synthesis of benzimidazoles and azabenzimidazoles
    发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARÉ MARC; URMANN MATTHIAS; HALLAND NIS; RKYEK OMAR
    权利人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARÉ MARC; URMANN MATTHIAS; HALLAND NIS; RKYEK OMAR; SANOFI SA
    摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, n nwherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct copper catalyzed regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides.

    专利号:EP-2173747-B1
    优先权日:2007-06-26
    标 题:A regioselective metal catalyzed synthesis of annelated benzimidazoles and azabenzimidazoles
    发明人:ALONSO JORGE; LINDENSCHMIDT ANDREAS; NAZARE MARC; R KYEN OMAR; URMANN MATHIAS; HALLAND NIS
    权利人:SANOFI SA
    摘要:The present invention relates to a process for the regioselective synthesis of compounds of the formula I, wherein R1; R2; R3; R4; J1; J2; J3; J4 and G have the meanings indicated in the claims. The present invention provides a direct metal, e.g. palladium or copper, catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides.

    专利号:US-4711957-A
    优先权日:1979-07-13
    标题 :Synthesis of 2-keto-1,4-diazacycloalkanes
    发明人:LAI JOHN T
    权利人:GOODRICH CO B F
    摘要:The disclosure deals with novel synthesis involving (a) hydrogenation of a cis-3,3-dialkyl-3,4-dihydroquinoxaline-2-one in the presence of a suitable hydrogenation catalyst, at elevated temperature and pressure, to yield a cis-3,3-dialkyl decahydroquinoxaline-2-one; (b) reaction of trans-1,2-diaminocyclohexane with acetone cyanohydrin in the presence of water to yield trans-3,3-dimethyl-decahydroquinoxaline-2-one; and (c) a reaction of 1,2-diamine with a saturated acyclic or cyclic monoketone or aldehyde and a holoform, in the presence of (i) a phase transfer catalyst (ii) an organic solvent, and (iii) solid or aqueous alkali to yield 2-keto-1,4-diazacycloalkanes. Such compounds exhibit exceptional UV light stabilizing property.

    专利号:US-6413957-B1
    优先权日:1998-04-21
    标题:Methods of inhibiting cell proliferation using indeno [1,2-c]pyrazol-4-ones
    发明人:NUGIEL DAVID A; CARINI DAVID J; DI MEO SUSAN V; YUE EDDY W
    权利人:BRISTOL MYERS SUIBB PHARMA COM
    摘要:The present invention relates to the synthesis of a new class of indeno[1,2-c]pyrazol-4-ones of formula (I): n that are potent inhibitors of the class of enzymes known as cyclin dependent kinases, which relate to the catalytic subunits cdk1-7 and their regulatory subunits know as cyclins A-G. This invention also provides a novel method of treating cancer or other proliferative diseases by administering a therapeutically effective amount of one of these compounds or a pharmaceutically acceptable salt form thereof. Alternatively, one can treat cancer or other proliferative diseases by administering a therapeutically effective combination of one of the compounds of the present invention and one or more other known anti-cancer or anti-proliferative agents.

    专利号:US-4806648-A
    优先权日:1986-12-18
    标题 :Efficient synthesis of cyclic cis-vicinal teritiary diamines
    发明人:ROSENZWEIG HOWARD; FRAENKEL GIDEON
    权利人:UNIV OHIO STATE RES FOUND
    摘要:The one aspect of this invention relates to a process for making cis-vicinal tertiary diamines of general formula: ##STR1## wherein n is from 2-8, and NR 21 is selected from a group including N-piperidino, N-pyrrolidino, dialkylamino containing C 1 -C 12 straight or branched alkyl groups optionally substituted by C 3 -C 7 cycloalkyl groups. The process comprises the formation of a cyclic aminoenamine and the stereospecific catalytic hydrogenation of cyclic aminoenamine to a cis diamine. Another aspect of this invention involves the uses of cis-vicinal tertiary diamines as catalysts of organolithium initiated anionic polymerization of 1,3-dienes, as anti-neoplastic agents and as bacteriacides.

    专利号:US-2006025421-A1
    优先权日:2004-06-25
    标 题:Pyridyl piperazines for the treatment of CNS disorders
    发明人:BRODNEY MICHAEL A
    权利人:PFIZER
    摘要:This invention is directed to compounds of Formula I and to pharmaceutical compositions comprising the compound of Formula I. n n where the dashed line represents an optional double bond; and where n is 1 or 2, and Ar 1 , Ar 2 , . . . and Z are as defined in the specification. The invention is also directed to a method of treating a disorder or condition that can be treated by altering serotonin-mediated neurotransmission, such as migraine, headache, cluster headache, anxiety, depression, etc. This invention is also directed to intermediates useful in the synthesis of compounds of Formula I.
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    摘要:Seidel, D., Science of Synthesis Knowledge Updates, (2012) 3, 427.
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