CAS: 146862-02-4; (4-(Trans-4-Propylcyclohexyl)Phenyl)Boronic Acid

该化合物是有机体化合物,其特征是附于一个苯环上的碱酸功能组,该组又被一个跨丙环环己基组所取代.该化合物通常具有与乙酸相关的特性,例如能够形成可逆的共价结合,与二醇形成可逆转的共值结合,使其在包括有机合成和材料科学在内的各种应用中有用.聚丙环乙酰乙烯组的存在可以影响其溶解性和性能,有可能加强其在苏祖基-米亚乌拉交织等交叉反应中的再活动.此外,氨酸因其在药用化学中的作用而闻名,特别是在针对特定生物路径开发药品方面.该混合物的结构特征还可能具有独特的物理特性,如熔点和沸点,而这些是其实际应用所必不可少的.总体而言,[4-(TRNS-4-N-PROPLICLUEXYYYLYL)PHENL] PHONIC ACINCI ACI ASYL ACYL是合成有机化学中一个多功能化建筑块.

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156837-90-0 143651-26-7 374538-04-2

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ECHA物质C&L通报

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    专利号:CN-114671744-A
    优先权日:2020-12-24
    标 题 :A Green Method for Synthesis of Compounds Containing Biaryl Structures by Suzuki Coupling Reaction

    专利号:CN-114671745-A
    优先权日:2020-12-24
    标题 :A Green Method for Synthesis of Compounds Containing Biaryl Structures by Suzuki Coupling Reaction

    专利号:US-9795613-B2
    优先权日:2014-12-10
    标题 :GLP-1 receptor modulators
    发明人:BOEHM MARCUS F; MARTINBOROUGH ESTHER; MOORJANI MANISHA; TAMIYA JUNKO; HUANG LIMING; YEAGER ADAM R; BRAHMACHARY ENUGURTHI; FOWLER THOMAS; NOVAK ANDREW; MEGHANI PREMJI; KNAGGS MICHAEL; GLYNN DANIEL; MILLS MARK
    权利人:CELGENE INT II SÀRL
    摘要:Compounds are provided that modulate the glucagon-like peptide 1 (GLP-1) receptor, as well as methods of their synthesis, and methods of their therapeutic and/or prophylactic use. Such compounds can act as modulators or potentiators of GLP-1 receptor on their own, or with incretin peptides such as GLP-1(7-36) and GLP-1(9-36), or with peptide-based therapies, such as exenatide and liraglutide, and have the following general structure (where “ â€? represents either or both the R and S form of the compound): n nwhere A, B, C, Y 1 , Y 2 , Z, R 1 , R 2 , R 3 , R 4 , R 5 , W 1 , n, p and q are as defined herein.

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