CAS: 108238-09-1; 2-Phenoxybenzeneboronic Acid

相似化合物

1056372-58-7 51067-38-0 221006-66-2

上下游产品

CAS号101-84-8 二苯醚 | CAS号121-43-7 硼酸三甲酯 | CAS号2216-12-8 2-硝基苯基苯基醚 | CAS号2417-10-9 2-羟基二苯醚 | CAS号6738-04-1 2-苯氧基联苯

📜二苯醚置于正丁基锂,硼酸三甲酯,盐酸体系中,用 四氢呋喃,水 用作溶剂,化学反应 2.5H,反应生成2-苯氧基苯硼酸
参考文献:Intracellular Calcium Concentration Increase Inhibitors
标题:Intracellular Calcium Concentration Increase Inhibitors
摘要:一种含有活性成分的细胞内钙浓度增加抑制剂,其活性成分为(1)由化学式(i)表示的硼化合物.化学式(i)表示的化合物抑制细胞内钙浓度的增加,因此被认为可用作预防和/或治疗血小板聚集,心脑缺血疾病,免疫缺陷疾病,变态反应,支气管哮喘,高血压,脑血管痉挛,各种肾脏疾病,胰腺炎,阿尔茨海默病等的药物.

专利信息

专利号:US-8207337-B2
优先权日:2007-01-29
标 题:Reagent for organic synthesis reaction containing organic triol borate salt
发明人：MIYAURA NORIO; YAMAMOTO YASUNORI
权利人:MIYAURA NORIO; YAMAMOTO YASUNORI; WAKO PURE CHEM IND LTD
摘要:[Problem] n To provide an organoboron compound-containing reagent for organic synthesis reactions which undergoes no trimerization with dehydration, does not necessitate activation with a base, and is stable and highly active. n [Means for Solving Problems] n The reagent for organic synthesis reactions contains an organic triol borate salt represented by any of the general formulae (I) to (III) and general formula (XVI): (wherein R 1 represents alkyl, alkenyl, etc.; R 2 represents optionally substituted alkyl, alkenyl, alkynyl, etc. or represents hydrogen; m + represents an alkaline metal ion, phosphonium ion, or given ammonium ion; M 2+ represents an alkaline earth metal; X represents halogen or alkoxide; Y represents an alkali metal ion, etc.; A represents optionally substituted methylene; and n represents an integer).

专利号:US-2009069334-A1
优先权日:2007-08-18
标题:Pyridazine based alpha-helix mimetics
发明人：REBEK JR JULIUS; BIROS SHANNON; MOISAN LIONEL; VOLONTERIO ALESSANDRO; MANN ENRIQUE; DALE TREVOR
权利人:SCRIPPS RESEARCH INST
摘要:The synthesis of new α-helix scaffolds mimicking i, i+3 or i+4, i+7 residues, was accomplished. The common pyridazine heterocycle originates from the easily available building block, 6. These scaffolds may be thought of as synthetic counterparts of amphiphilic α-helices having a “wet face†along one side and a hydrophobic face along the other side of the helix.

专利号:US-2022204495-A1
优先权日:2019-05-03
标题:Inhibiting trabid
发明人：CAMPBELL ANNE-MARIE; MARCIN Lawrence; KAYSER-BRICKER KATHERINE
权利人:VALO HEALTH INC; INTEGRAL HEALTH HOLDINGS LLC
摘要:The present disclosure is directed to compounds of formulas (I)-(VII), which are useful as modulators of TRABID. The compounds are further useful in the inhibition of TRABID and the treatment of diseases or disorders associated with the inhibition of TRABID. For instance, the disclosure is concerned with compounds and compositions for inhibition of TRABID, methods of treating diseases associated with the inhibition of TRABID (e.g., autoimmune inflammatory diseases including, but not limited to, psoriasis), and methods of synthesis of these compounds.

专利号:CA-2965558-A1
优先权日:2014-10-30
标题 :Synthesis of substituted 1h-pyrazolo[3,4-d]pyrimidines

专利号:EP-3212624-A1
优先权日:2014-10-30
标 题 :Synthesis of substituted 1h-pyrazolo[3,4-d]pyrimidines

专利号:CN-106795124-A
优先权日:2014-10-30
标题 :Synthesis of Substituted 1H-pyrazolo[3,4-d]pyrimidines