CAS: 28425-04-9; Dichloro Bis(Triethylphosphine) Palladium(Ii)

该化合物是一个协调化合物,在+2氧化状态下以为特征,其特点是与两种氯化离子和两种三乙硫酸相协调,以其强大的电子施食特性而著称.中心通常展示平方平方平面几何,这是D8金属综合体的共同安排.该化合物经常被用作各种有机反应的催化剂,特别是苏木和赫克反应等交叉反应的催化剂,因为它能够促进形成碳-碳联结.其在有机溶剂中的溶解性使其适合用于多种合成用途.此外,三乙乙硫离子的出现可以增强中心的稳定性和再活性.在处理该化合物时,应当考虑到安全因素,因为如果是吸入或吸入,可能会对健康造成风险,因此在适当的实验室安全议定书应当得到遵守.

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CAS号12107-56-1 (1,5-环辛二烯)氯化钯(II) | CAS号110-60-1 1,4-丁二胺 | CAS号40927-17-1 2,2,2-trifluoro... | CAS号10025-98-6 氯亚钯酸钾 | CAS号554-70-1 三乙基膦 | CAS号33410-18-3 n,π-(chloro)2(3... | CAS号15638-57-0 palladium(2+),t...

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    专利信息


    专利号:US-2024294532-A1
    优先权日:2021-07-12
    标题 :Synthesis of chiral substituted pyrazolopyrimidine compounds
    发明人:TOMAS LOÃ?C; HARRIS CRAIG STEVEN
    权利人:GALDERMA HOLDING S A
    摘要:The present invention relates to processes and intermediates for the preparation of compounds useful as inhibitors of mechanistic target of rapamycin (mTOR).

    专利号:US-5663397-A
    优先权日:1995-09-14
    标 题 :Cyclic silyl enol ethers and method of preparing the same
    发明人:YAMASHITA HIROSHI; TANAKA MASATO
    权利人:AGENCY IND SCIENCE TECHN
    摘要:There is disclosed a method of preparing cyclic silyl enol ethers (1-oxa-2-sila-5-cyclohexenes), comprising reacting a silacyclobutane with an acid halide in the presence of a palladium catalyst and an organic base. There is also disclosed novel cyclic silyl enol ethers obtained by the above method. The above cyclic silyl enol ethers belong to a new class of silyl enol ethers which are useful in the production of medicines and agricultural chemicals, and they can be used as intermediates of fine chemicals or as various reagents for fine synthesis.

    专利号:EP-4370517-A1
    优先权日:2021-07-12
    标题 :Synthesis of chiral substituted pyrazolopyrimidine compounds

    专利号:CN-110204558-B
    优先权日:2014-08-15
    标 题:Synthesis of cephalosporin compounds

    专利号:WO-2023285926-A1
    优先权日:2021-07-12
    标题 :Synthesis of chiral substituted pyrazolopyrimidine compounds

    专利号:US-11459325-B2
    优先权日:2018-01-31
    标题:Heterocyclic compound
    发明人:TANAKA YUTA; OHASHI TOMOHIRO; IKEDA ZENICHI; TANAKA YUTA; PÜNNER FLORIAN; YAMAMOTO TAKESHI; KAKEGAWA KEIKO; KIKUCHI FUMIAKI; MORISHITA NAO; KASAHARA TAKAHITO; SETO MASAKI; NAKAMURA MINORU; TAKAMI KAZUAKI; MURAKAMI MASATAKA; DAINI MASAKI; MIKAMI SATOSHI; SASAKI MINORU
    权利人:TAKEDA PHARMACEUTICALS CO
    摘要:The present invention provides a compound having a glucosylceramide lowering action (e.g., promoting glucosylceramide metabolism, inhibition of glucosylceramide synthesis, promoting glucosylceramide catabolism, etc.), which is expected to be useful as an agent for the prophylaxis or treatment of lysosome diseases (e.g., Gaucher's disease), neurodegenerative diseases (e.g., Parkinson's disease, Lewy body dementia, multiple-system atrophy) and the like. n The present invention relates to a compound represented by the formula (I): n nwherein each symbol is as described in the specification, or a salt thereof.

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    合成参考文献


    摘要:Marschner, C.; Baumgartner, J., Science of Synthesis Knowledge Updates, (2013) 2, 110.
    摘要:Denmark, S.; Chang, W.-T. T., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 1, 470.
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