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CAS登录号 中文名 英文名 分子结构式 分子式 详情 供应商
108983-83-11-Piperazineethanol,4-(diphenylmethyl)-, hydrochloride (1:2);
1-Piperazineethanol,4-diphenylmethyl-, dihydrochloride (6CI);
4-Benzhydryl-1-piperazineethanoldihydrochloride
CAS:108983-83-1分子结构C19H26Cl2N2O详情供应商
7468-39-53-Pentanone,1,5-bis(methylamino)-2,4-diphenyl-, dihydrochloride (8CI);
NSC 400776
CAS:7468-39-5分子结构C19H26Cl2N2O详情供应商
83913-06-8TRANS -(+/-)-3,4-DICHLORO-N-METHYL-N-(2-[1-PYRROLIDINYL]CYCLOHEXYL) BENZENEACETAMIDE;
dichloromethyl-2-(1-pyrrolidinyl)cyclohexyl derivative
CAS:83913-06-8分子结构C19H26Cl2N2O详情供应商
67198-13-4trans-(-3,4-Dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamidehydrochloride;
U50,488;
2-(3,4-dichlorophenyl)-N-methyl-N-(2-pyrrolidin-1-ylcyclohexyl)acetami de;
3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer;
U-50488 mesylate (±)-;
trans-(±)-3,4-Dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide mesylate;
rel-3,4-Dichloro-N-methyl-N-[(1α*)-2β*-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide;
3,4-Dichloro-N-methyl-N-[(1β,2α)-2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide;
3,4-Dichloro-N-methyl-N-[2α-(pyrrolidin-1-yl)cyclohexan-1β-yl]benzeneacetamide
CAS:67198-13-4分子结构C19H26Cl2N2O详情供应商
1346233-68-83,5-Dichloro-N-[[(1α,5α,6-exo,6α)-3-(3,3-diMethylbutyl)-3-azabicyclo[3.1.0]hex-6-yl]Methyl]-benzaMideCAS:1346233-68-8化学结构C19H26Cl2N2O详情供应商
热门搜关键词:5-bromofuran-2-carboxylic 2,3,4-Trihydroxybenzoic 5-TRIFLUOROMETHYL-PYRIDINE-3-BORONIC DL-3,4-dihydroxymandelic 3,5-bis(trifluoromethyl)benzeneboronic 1-Cyclopropyl-6,7-Difluoro-1,4-Dihydro-8-Methoxy-4-Oxo-3-Quinolinecarboxylic 18/5000 氢二钠 c4h602. c2h4 羟基 萘甲酸 C17H18O2 19825-73-1 Propenal, MOPIP C25N2H22 C8H4NOF C23H29 C23H29Br C23H26Br C23H27Br C23H28Br RAB1 4(1H)-吡啶酮 苯二甲酸 羟基苯甲酸 萘 羟基苯甲酸 萘 苯甲酸 IRF4 5-cyanothiophene-2-boronic BIS(4-CHLOROPHENYL)ACETI furan-2,5-dicarboxylic 脂肪酸锰盐 3-cyano-5-methyl Blue 1 nicotyri CH3CH2CHCH3CH2CH2CH2CH2CH3 C8N2H22Si CH3CHCH3CH2CH2CH(CH3)2 C8O3H22N2Si CH3CH2CHCH3CH2CH2CH(CH3)2 CH3CHCHC(CH3)CHCOOH HOOCCH2C(CH3)2CH2COOH CH3CH2CH(CH3)CH2CH2CH(CH3)2