CAS: 677-43-0; N,N-Dimethylphosphoroamidic Dichloride

该化合物是有机磷化合物,其特征是磷状结构,一般是无色的黄色液体,以反应作用著称,特别是由于存在氯原子,可参与核循环替代反应.该化合物在有机溶剂中可溶解,但水溶性有限.该化合物主要用于合成各种含磷化合物,并用作生产农用化学品和药品的中间体.二甲基二氯化二,因其潜在毒性而得到承认,应谨慎处理,因为它可能会对皮肤,眼睛和呼吸系统造成刺激.适当的安全措施,包括使用个人防护设备,在与该物质合作时至关重要.其化学特性使它成为有机合成中有价值的试剂,特别是在发展生物活动化合物的过程中.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

N,N-dimethylammonium chloride N,N,N',N'-Tetramethylphosphorodiamidic chloride dimethyl amine bis-(dimethylamino)methanedimefox N,N,N',N'-Tetramethylphosphorodiamidic chloride N,N-dimethyl-N',N''-diphenyl-phosphamideN,N-dimethyl-N',N''-diphenyl-phosphamide N,N-dimethyl-N',N'-diphenylphosphorodihydrazidic

合成工艺路线路线简述

    📜N,N-Dimethylamidotetrachlorophosphorane置于二氧化硫体系中,用 乙醚 作为反应溶剂,以91.3%的收率获得产物n,N-二甲基磷氨基二氯化物
    参考文献:Reaction Of 1,1-Dichloro-1-Nitrosobutane With N,N-Dimethylamidodichlorophosphite
    标题:Reaction Of 1,1-Dichloro-1-Nitrosobutane With N,N-Dimethylamidodichlorophosphite
    摘要:
    DOI:10.1007/bf00957179

    海关参考信息

    专利信息


    专利号:US-12012427-B2
    优先权日:2019-10-31
    标 题 :Synthesis of Fmoc-protected morpholino monomers and their use in the synthesis of morpholino oligomer
    发明人:SINHA SURAJIT; KUNDU JAYANTA; GHOSH UJJWAL
    权利人:INDIAN ASS FOR THE CULTIVATION OF SCIENCE
    摘要:Present invention relates to stable Fmoc protected Morpholino monomers and corresponding oligonucleotides (PMO) and efficient synthesis of the same involving chlorophosphoramidate and H-Phosphonate chemistry. Successful syntheses of the oligonucleotide with higher yield and lesser time have been accomplished employing solid phase synthesis and easy deprotection of Fmoc group with Piperidine.

    专利号:US-8076476-B2
    优先权日:2007-11-15
    标 题 :Synthesis of morpholino oligomers using doubly protected guanine morpholino subunits
    发明人:REEVES MATTHEW DALE; WELLER DWIGHT D; LI YONGFU
    权利人:REEVES MATTHEW DALE; WELLER DWIGHT D; LI YONGFU; AVI BIOPHARMA INC
    摘要:Morpholino compounds are provided having the structure: n nwheren R 1 is selected from the group consisting of lower alkyl, di(lower alkyl)amino, and phenyl; R 2 is selected from the group consisting of lower alkyl, monocyclic arylmethyl, and monocyclic (aryloxy)methyl; R 3 is selected from the group consisting of triarylmethyl and hydrogen; and Y is selected from the group consisting of: a protected or unprotected hydroxyl or amino group; a chlorophosphoramidate group; and a phosphorodiamidate linkage to the ring nitrogen of a further morpholino compound or a morpholino oligomer. Such compounds include doubly protected morpholino guanine (MoG) monomers. Also described is their use in synthesis of morpholino oligomers.

    专利号:US-2021130379-A1
    优先权日:2019-10-31
    标题 :Synthesis of fmoc-protected morpholino monomers and their use in the synthesis of morpholino oligomer

    专利号:WO-2009064471-A1
    优先权日:2007-11-15
    标 题:Method of synthesis of morpholino oligomers

    专利号:CA-2704261-A1
    优先权日:2007-11-15
    标题:Method of synthesis of morpholino oligomers

    专利号:US-2011098483-A1
    优先权日:2008-03-27
    标题 :Substituted Nitrogen Heterocycles and Synthesis and Uses Thereof
    发明人:PETASIS NICOS A; MYSLINSKA MALGORZATA
    权利人:UNIV SOUTHERN CALIFORNIA
    摘要:The invention relates to a nitrogen heterocycle compound of formula 1: n n n n n n n n n n Also disclosed are a method of synthesizing the compound and use of the compound for treating various diseases and conditions.

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Wicha, J., Science of Synthesis, (2009) 48, 187.
    摘要:Wicha, J., Science of Synthesis, (2009) 48, 187.
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