CAS: 22996-21-0; 4-Methoxy-2-Nitrobenzaldehyde

上下游产品

CAS号17484-36-5 4-甲基-3-硝基苯甲醚 | CAS号123-11-5 4-甲氧基苯甲醛; 对甲氧基苯... | CAS号38469-83-9 2-硝基-4-甲氧基苯腈 | CAS号22996-23-2 4-甲氧基-2-硝基苄醇 | CAS号57559-52-1 1-(溴甲基)-4-甲氧基-2-硝基苯 | CAS号5344-78-5 4-溴-3-硝基苯甲醚 | CAS号75-17-2 甲醛肟(10%的水溶液,约2.... | CAS号96-96-8 冰染重氮组分 1 | CAS号33844-21-2 4-甲氧基-2-硝基苯甲酸 | CAS号100193-41-7 2-Nitro-4-metho... | CAS号22996-23-2 4-甲氧基-2-硝基苄醇 | CAS号187731-65-3 2-氨基-4-甲氧基苯甲醇 | CAS号23981-26-2 7-甲氧基-2-喹诺酮 | CAS号33844-21-2 4-甲氧基-2-硝基苯甲酸 | CAS号141080-74-2 2-[(18)F]-fluor... | CAS号57559-52-1 1-(溴甲基)-4-甲氧基-2-硝基苯 | CAS号531-59-9 7-甲氧基香豆素 | CAS号90151-04-5 4-羟基-2-硝基苯甲醛 | CAS号59236-36-1 2-氨基-4-甲氧基苯甲醛 | CAS号61063-01-2 4-methoxy-3-oxi...

4-甲氧基-2-硝基溴苄置于tetra(N-Butyl)Ammonium Dichromate(Vi)体系中,用 氯仿 用作溶剂,化学反应 8.0H,以75%的收率获得4-甲氧基-2-硝基苯甲醛
参考文献:笼状辣椒素的模型化合物:设计,合成和光反应性.
标题:笼状辣椒素的模型化合物:设计,合成和光反应性.
摘要:制备具有通过醚或碳酸酯键与n-(4-羟基-3-甲氧基苄基)乙酰胺(2)共价键合的取代硝基苄基的分子.这些化合物在363Nm的辐射下分解.具有碳酸酯键的那些分解速率比具有醚键的那些分解速率慢.由于苄基碳的电子特性,具有二甲氧基取代的苄基的分子比单甲氧基取代的苄基分解得更慢.
Doi:10.1021/jo034616T

专利信息

专利号:US-2010075297-A1
优先权日:2006-12-20
标题 :Photosensitive polypeptide and methods of their production and use
发明人：LAWRENCE DAVID S
权利人:LAWRENCE DAVID S
摘要:Methods for producing polypeptides caged with a photolabile group on one or more backbone nitrogens are provided, in which the photolabile group is added to a growing polypeptide chain during polypeptide synthesis. Photosensitive polypeptides produced by the methods are described, as are methods of using such photosensitive polypeptides to assay enzyme activity or inhibit protein-protein interactions. Methods for producing polypeptides caged with a photolabile group on one or more side chain nitrogens, where the photolabile group is incorporated into the side chain during polypeptide synthesis, are also provided.

专利号:US-8927569-B2
优先权日:2007-07-19
标 题 :Macrocyclic compounds as antiviral agents
发明人：HARPER STEVEN; SUMMA VINCENZO; LIVERTON NIGEL J; MCCAULEY JOHN A; BUTCHER JOHN W; DI FILIPPO MARCELLO; DI FRANCESCO MARIA EMILIA; FERRARA MARCO; ROMANO JOSEPH J; RUDD MICHAEL T
权利人:HARPER STEVEN; SUMMA VINCENZO; LIVERTON NIGEL J; MCCAULEY JOHN A; BUTCHER JOHN W; DI FILIPPO MARCELLO; DI FRANCESCO MARIA EMILIA; FERRARA MARCO; ROMANO JOSEPH J; RUDD MICHAEL T; MERCK SHARP & DOHME
摘要:A class of macrocyclic compounds of formula (I), wherein R 1 , R 3 , R 4 , R a , R b , A, Z, Y, X, M, W, n and m are defined herein, that are useful as inhibitors of viral proteases, particularly the hepatitis C virus (HCV) NS3 protease, are provided. Also provided are processes 5 for the synthesis and use of such macrocyclic compounds for treating or preventing HCV infection. Formula (I):

专利号:WO-2004052875-A1
优先权日:2002-12-05
标 题:Tyrostatin and related anticancer drugs
发明人：PETTIT GEORGE R; ANDERSON COLLIN R
权利人:UNIV ARIZONA STATE; PETTIT GEORGE R; ANDERSON COLLIN R
摘要:The present invention relates to novel compounds having antineoplastic activity, and methods for their synthesis. The compounds are of the formula (I) wherein R is selected from the group consisting of NH2, NH3Cl, NH-Cys, NH-Gly, NH-Phe, NH-Ser, NH-Trp, NH-Tyr, and NH-Val, and pharmaceutically acceptable salts thereof.