CAS: 165047-24-5; 2,4,5-Trifluorobenzaldehyde

相似化合物

144284-25-3 446-17-3 98349-22-5

上下游产品

CAS号165047-23-4 2-氯-4,5-二氟苯甲醛 | CAS号144284-25-3 2,4,5-三氟苯甲醇 | CAS号1839-72-1 2-苯基-1-苯并呋喃 | CAS号4461-52-3 甲氧基甲醇 | CAS号486460-08-6 (R)-N-叔丁氧羰基-2,4...

2-氯-4,5-二氟苯甲醛 反应生成2,4,5-三氟苯甲醛
参考文献:Process For Preparing 4,5-Difluorobenzaldehydes
标题:Process For Preparing 4,5-Difluorobenzaldehydes
摘要:给定的化学式4,5-二氟苯甲醛是通过对应的苯甲醛与氟化试剂的反应制备的.

专利信息

专利号:US-8765668-B2
优先权日:2010-06-04
标 题 :Methods of synthesis of β-aminobutyryl substituted compounds
发明人：STERK DAMJAN; USTAR MATJAZ; ZLICAR MARKO
权利人:STERK DAMJAN; USTAR MATJAZ; ZLICAR MARKO; LEK PHARMACEUTICALS
摘要:The present invention relates to process to prepare β-aminobutyryl compounds having β-amino acid core structural moieties and optionally having γ-phenyl and/or heterocyclic structural moieties. Such compounds are useful as key structure framework of modern drug chemistry.

专利号:US-5574146-A
优先权日:1994-08-30
标题:Oligonucleotide synthesis with substituted aryl carboxylic acids as activators
发明人：REDDY M PARAMESWARA; FAROOQUI FIRDOUS
权利人:BECKMAN INSTRUMENTS INC
摘要:A process for synthesizing oligonucleotides by phosphoramidite chemistry wherein the improvement is the use of substituted aryl carboxylic acids as the activators. These activators produce in situ nucleotide intermediates in which the substituted arylcarbonyl group has displaced the amidite moiety.

专利号:US-6245773-B1
优先权日:1996-05-16
标题:5-(heterocyclic alkyl)-6-aryl-dihydropyrimidines
发明人：WONG WAI C; LAGU BHARAT; NAGARATHNAM DHANAPALAN; MARZABADI MOHAMMAD R; GLUCHOWSKI CHARLES
权利人:SYNAPTIC PHARMA CORP
摘要:This invention is directed to dihydropyrimidine compounds of the following formula: n which are selective antagonists for human α 1A receptors. This invention is also related to uses of these compounds for lowering intraocular pressure, inhibiting cholesterol synthesis, relaxing lower urinary tract tissue, the treatment of benign prostatic hyperplasia, impotency, cardiac arrhythmia and for the treatment of any disease where antagonism of the α 1A receptor may be useful. The invention further provides a pharmaceutical composition comprising a therapeutically effective amount of the above-defined compounds and a pharmaceutically acceptable carrier.

专利号:US-6727257-B1
优先权日:1994-11-16
标题 :5-(heterocyclic alkyl)-6-aryl-dihydropyrimidines
发明人：NAGARATHNAM DHANAPALAN; CHIU GEORGE; DHAR T G MURALI; WONG WAI C; MARZABADI MOHAMMAD R; GLUCHOWSKI CHARLES; LAGU BHARAT; MIAO SHOU WU
权利人:SYNAPTIC PHARMA CORP
摘要:This invention is directed to dihydropyrimidine compounds of the following formula: n wherein A is n which are selective antagonists for human α 1C receptors. This invention is also related to uses of these compounds for lowering intraocular pressure, inhibiting cholesterol synthesis, relaxing lower urinary tract tissue, the treatment of benign prostatic hyperplasia, impotence, cardiac arrhythmia and for the treatment of any disease where antagonism of the α 1C receptor may be useful. The invention further provides a pharmaceutical composition comprising a therapeutically effective amount of the above-defined compounds and a pharmaceutically acceptable carrier.

专利号:CN-105017099-A
优先权日:2015-07-15
标题 :A kind of sitagliptin chiral intermediate and asymmetric synthesis method