CAS: 22532-62-3; 4-Bromo-2-Hydroxybenzaldehyde

上下游产品

chloroform 3-Bromophenol Bromoform 2-amino-4-bromobenzaldehyde 5-bromo-2-formylphenyl acetate N-benzothiazol-2-yl-4-(4-bromo-2-hydroxy-benzylideneamino)-benzenesulfonamideN-benzothiazol-2-yl-4-(4-bromo-2-hydroxy-benzylideneamino)-benzenesulfonamide 4-Bromo-2-(4-nitro-benzyloxy)-benzaldehyde 4-(2-Methyl-imidazo[1,2-a]pyridin-3-ylazo)-benzoic acid [1-(4-bromo-2-hydroxy-phenyl)-meth-(E)-ylidene]-hydrazide

2-氨基-4-溴苯甲醛 反应生成4-溴-2-羟基苯甲醛
参考文献:Mueller,J.,Chemische Berichte,1909,Vol. 42,P. 3697
标题:Mueller,J.,Chemische Berichte,1909,Vol. 42,P. 3697

专利信息

专利号:WO-2025077857-A1
优先权日:2023-10-13
标题:Use of prmt5 inhibitor in treatment of tumors or cancers
发明人：YAO BING; GU XIAOHUI; MAO WEIFENG; ASWAD FRED JULLIEN; JOSEPH JAMES DAVID; LI MINGXI
权利人:SHANGHAI APEIRON THERAPEUTICS COMPANY LTD
摘要:The present disclosure describes a novel molecule having protein arginine methyltransferase 5 inhibitory activity, and methods for synthesis and use of a compound. Specifically, the present disclosure describes a compound of formula (I) or a pharmaceutically acceptable salt, hydrate or solvate thereof, and methods for synthesis and use of the compound.

专利号:US-3957760-A
优先权日:1970-12-16
标 题:Amino acid derivatives
发明人：BODANSZKY MIKLOS
权利人:SQUIBB & SONS INC
摘要:New lactone intermediates useful in the synthesis of peptides are prepared by reacting an α-amino acid with an active carbonyl compound which forms a Schiff's base. The latter is treated with a condensing agent so that cyclization occurs and a lactone is formed from which a peptide may be produced by reaction with an amino acid ester and removal of the protecting groups.

专利号:US-2987525-A
优先权日:1958-10-29
标题:Synthesis of polycyclic heterocyclic compounds
发明人：ARRIGO JOSEPH T
权利人:UNIVERSAL OIL PROD CO

专利号:US-2018065917-A1
优先权日:2016-09-02
标 题 :Immune checkpoint inhibitors, compositions and methods thereof
发明人：WEBBER STEPHEN E; ALMASSY ROBERT J
权利人:POLARIS PHARMACEUTICALS INC
摘要:The present invention provides synthesis, pharmaceutically acceptable formulations and uses of compounds in accordance with Formula (I), or a stereoisomer, a tautomer or a pharmaceutically acceptable salt thereof. n n n n n n n n n n For Formula (I) compounds R 1 , R 2 , X 1 , Y 1 and n are as defined in the specification. The inventive Formula (I) compounds are inhibitors of the PD-1/PD-L1 protein/protein binding or functional interaction and find utility in any number of therapeutic applications, including but not limited to treatment of proliferative disorders such as cancer and infectious diseases.

专利号:CN-120157598-A
优先权日:2023-12-15
标 题 :Synthesis method of dihydrobenzofuran derivative

专利号:CN-117304067-A
优先权日:2022-06-21
标 题 :Synthesis method of non-nefardone intermediate 4-cyano-2-methoxybenzaldehyde