CAS: 702-24-9; 4-Methoxy-N-Methylbenzylamine

该化合物是一种有机化合物,其特点是其有矿物质功能组和甲氧替代组,其特点是一个苯环,其甲氧基组(-OCH3)位于相对于该矿物质组(-NH(CH3)-)的准位置.该化合物一般是无色的,可粉黄液体或固体,视其纯度和形态而定.有机溶剂中可以溶解,并显示出中度极性,因为存在缺水芳烃和水合金和甲基氧组.N-Me乙基-4-meththoxybenzylamine经常用于有机合成,并可作为生产制药或农用化学品中的中间体.其再活性受甲氧基氧基组的电饱和性影响,可增强核糖分泌性.在处理时,应参考安全数据,因为氨酯可以是刺激剂,并可能构成健康风险.总的来说,这种化合物在各种化学应用中是其结构特性和再活动.

结构式图片

欧盟法规

REACH注册ECHA物质C&L通报

上下游产品

CAS号123-11-5 4-甲氧基苯甲醛; 对甲氧基苯... | CAS号74-89-5 氨基甲烷 | CAS号824-94-2 4-甲氧基苄氯 | CAS号13114-23-3 N-(4-甲氧基亚苄基)甲胺 | CAS号5129-86-2 N-(4-methoxy-be... | CAS号2393-23-9 对甲氧基苄胺 | CAS号100-66-3 苯甲醚 | CAS号2746-25-0 4-甲氧基溴苄 | CAS号3400-22-4 4-甲氧基-N-甲基苯甲酰胺 | CAS号13114-23-3 N-(4-甲氧基亚苄基)甲胺 | CAS号1657-55-2 Benzene,1,1'-(1... | CAS号78507-19-4 4-[(甲氨基)甲基]苯酚 | CAS号84174-20-9 N-Methyl-N-nitr...

合成工艺路线路线简述

    N-[(1E)-(4-Methoxyphenyl)Methylene]Methanamine置于sodium Tetrahydroborate体系中,化学反应生成 N-甲基-4-甲氧基苄胺
    参考文献:A Mechanistic Approach To The Reaction Between Imines And Sodium Hydrogen Telluride
    标题:A Mechanistic Approach To The Reaction Between Imines And Sodium Hydrogen Telluride
    摘要:
    DOI:10.1016/s0040-4039(00)86114-6

    海关参考信息

    专利信息


    专利号:US-8188113-B2
    优先权日:2006-09-14
    标 题 :Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases
    发明人:FLYNN DANIEL L; PETILLO PETER A; KAUFMAN MICHAEL D; PATT WILLIAM C
    权利人:FLYNN DANIEL L; PETILLO PETER A; KAUFMAN MICHAEL D; PATT WILLIAM C; DECIPHERA PHARMACEUTICALS INC
    摘要:The present invention relates to novel dihydropyridopyrimidinyl, dihydronaphthyridinyl, and related compounds which are kinase inhibitors and modulator useful for the treatment of various diseases. More particularly, the invention is concerned with such compounds, kinase/compound adducts, methods of treating diseases, and methods of synthesis of the compounds. Preferably, the compounds are useful for the modulation of kinase activity of Raf kinases and disease polymorphs thereof. Compounds of the present invention find utility in the treatment of mammalian cancers and especially human cancers including but not limited to malignant melanoma, colorectal cancer, ovarian cancer, papillary thyroid carcinoma, non small cell lung cancer, and mesothelioma. Compounds of the present invention also find utility in the treatment of rheumatoid arthritis and retinopathies including diabetic retinal neuropathy and macular degeneration.

    专利号:WO-2023002323-A1
    优先权日:2021-07-19
    标 题 :Synthesis of substituted tricyclic amides and analogues thereof

    专利号:CN-117730082-A
    优先权日:2021-07-19
    标 题:Synthesis of substituted tricyclic amides and analogs thereof

    专利号:WO-2024256496-A1
    优先权日:2023-06-14
    标题 :[1,2,4]-triazolo[4,3-b]pyridazine derivatives useful as a medicament
    发明人:ELIE JONATHAN; GEORGE PASCAL; MIEGE FRÉDÉRIC; MEIJER LAURENT
    权利人:PERHA PHARMACEUTICALS
    摘要:The present invention relates to a compound of formula (I) or any of its pharmaceutically acceptable salt. The present invention further relates to a synthesis process for manufacturing compound of formula (I) or any of its pharmaceutically acceptable salts, comprising at least a step of reacting a compound of formula (II) with an amine of formula (IV) NHR5R6 for example in a molar ratio ranging from 1 to 20 eq, with respect to the compound of formula (II), in an aprotic solvent or without solvent or else in a protic solvent.

    专利号:RU-2119482-C1
    优先权日:1991-01-11
    标 题:Acridine derivatives, method of synthesis, pharmaceutical composition and a method of treatment of patients with malignant tumors

    专利号:US-9611264-B1
    优先权日:2015-09-24
    标 题:N-[2-(3-amino-2,5-dimethyl-1,1-dioxido-5,6-dihydro-2H-1,2,4-thiadiazin-5-yl)-1,3-thiazol-4-yl] amides
    发明人:BRODNEY MICHAEL AARON; BUTLER CHRISTOPHER RYAN; ZHANG LEI; O'NEILL BRIAN THOMAS; VERHOEST PATRICK ROBERT; SALOMON FERRER ROMELIA DEL CARMEN
    权利人:PFIZER
    摘要:The present invention is directed to compounds, tautomers and pharmaceutically acceptable salts of the compounds which are disclosed, wherein the compounds have the structure of Formula I, n n n n n n n n n n n n wherein the variables R 1 , R 2 and R 3 are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
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    合成参考文献


    摘要:D.H. Rosenblatt, L.A. Hull, D.C. DeLuca, G.T. Davis, R.C. Weglein and H.K.R. Williams. J. Am. Chem. Soc. 89, 1158 (1967).
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