CAS: 594-45-6; Ethanesulfonic Acid

相似化合物

304672-01-3 2495-39-8 598-59-4

上下游产品

CAS号110-81-6 二乙基二硫 | CAS号75-08-1 乙硫醇 | CAS号1184-84-5 乙烯基磺酸 | CAS号54509-73-8 ethene | CAS号542-90-5 硫氰酸乙酯 | CAS号75-03-6 碘乙烷 | CAS号74-96-4 溴乙烷 | CAS号14265-45-3 sulfur trioxide | CAS号64-17-5 乙醇 | CAS号594-44-5 乙基磺酰氯 | CAS号54509-73-8 ethene | CAS号123-43-3 磺基乙酸 | CAS号503-40-2 甲基二磺酸 | CAS号64-19-7 冰醋酸 | CAS号1912-30-7 乙烷磺酸乙酯 | CAS号1912-28-3 乙磺酸甲酯 | CAS号67-72-1 六氯乙烷 | CAS号594-44-5 乙基磺酰氯 | CAS号13223-06-8 ethanesulfonic ... | CAS号70284-09-2 N-diazoethanesu...

硫氰酸乙酯置于盐酸,溶剂黄146体系中,化学反应生成 乙基磺酸
参考文献:Fichter; Wenk,Chemische Berichte,1912,Vol. 45,P. 1374
标题:Fichter; Wenk,Chemische Berichte,1912,Vol. 45,P. 1374

专利信息

专利号:US-9643915-B2
优先权日:2013-03-15
标题:Methods for the synthesis of sphingomyelins and dihydrosphingomyelins
发明人：ONICIU DANIELA CARMEN; HECKHOFF STEFAN; OSWALD BENOIT; REBMANN PETER; PEER ANDREAS; GONZALEZ MIGUEL; SAUTER PATRIK
权利人:CERENIS THERAPEUTICS HOLDING SA
摘要:The present invention includes methods for the synthesis of sphingomyelins and dihydrosphingomyelins. The present invention also includes methods for the synthesis of sphingosines and dihydrosphingosines. The present invention further includes methods for the synthesis of ceramides and dihydroceramides.

专利号:US-9708354-B2
优先权日:2013-03-15
标 题:Methods for the synthesis of sphingomyelins and dihydrosphingomyelins
发明人：ONICIU DANIELA CARMEN; HECKHOFF STEFAN; OSWALD BENOIT; REBMANN PETER; PEER ANDREAS; GONZALEZ MIGUEL; SAUTER PATRIK
权利人:CERENIS THERAPEUTICS HOLDING SA
摘要:The present invention includes methods for the synthesis of sphingomyelins and dihydrosphingomyelins. The present invention also includes methods for the synthesis of sphingosines and dihydrosphingosines. The present invention further includes methods for the synthesis of ceramides and dihydroceramides.

专利号:US-7179919-B2
优先权日:2004-03-18
标 题 :Stereoselective synthesis of certain trifluoromethyl-substituted alcohols
发明人：SONG JINHUA J; TAN ZHULIN; YEE NATHAN K; SENANAYAKE CHRIS HUGH; XU JINGHUA; GALLOU FABRICE
权利人:BOEHRINGER INGELHEIM PHARMA
摘要:A process for stereoselective synthesis of a compound of Formula (I) n nwherein R 1 , R 2 , R 3 , R 4 , and R 5 are as described herein.

专利号:US-2007088174-A1
优先权日:2005-10-19
标 题 :Synthesis of phenoxyacetic acid derivatives
发明人：WINTER ERIC; REICHEL CARSTEN; GUTHEIL DIETER
权利人:BOEHRINGER INGELHEIM INT
摘要:The present invention relates to an improved process for the preparation of substituted 2-(4-carbonylmethoxy-optionally 2,5-disubstituted-phenyl)-acetaldehydes, in particular 2-(4-alkoxycarbonylmethoxy-optionally 2,5-disubstituted-phenyl)-acetaldehydes and their use in the synthesis of optionally substituted 2-[4-[2-[[-2-hydroxy-2-(4-hydroxyphenyl)-1-methylethyl]-amino]ethyl]-optionally 2,5-disubstituted-phenoxy]acetic acid derivatives or the salts thereof, which may be used as pharmaceutically active substances.

专利号:US-2009247781-A1
优先权日:2004-10-26
标 题:Synthesis of phenoxyacetic acid derivatives
发明人：WINTER ERIC; REICHEL CARSTEN; GUTHEIL DIETER
权利人:KISSEI PHARMACEUTICAL
摘要:The present invention relates to an improved process for the preparation of substituted 2-(4-carbonylmethoxy-optionally 2,5-disubstituted-phenyl-acetaldehydes, in particular 2-(4-alkoxycarbonylmethoxy-optionally 2,5-disubstituted-phenyl)-acetaldehydes and their use in the synthesis of optionally substituted 2-[4-[2-[[-2-hydroxy-2-(4-hydroxyphenyl)- 1 -methylethyl]-amino]ethyl]-optionally 2,5-disubstituted-phenoxy]acetic acid derivatives or the salts thereof, which may be used as pharmaceutically active substances.

专利号:US-6159673-A
优先权日:1996-07-17
标 题:Oxonol compound, light-sensitive material and process for the synthesis of oxonol compound
发明人：NISHIGAKI JUNJI; DEGUCHI YASUAKI
权利人:FUJI PHOTO FILM CO LTD
摘要:An oxonol compound is represented by the following formula (I): in which Z is an atomic group that forms a cyclic amide ring; each of W1 and W2 independently is an atomic group that forms an acidic nucleus ring; and M is a cation. Other oxonol compounds, a light-sensitive material containing an oxonol compound and a process for the synthesis of an oxonol compound are also disclosed.