所有图片(1)
别名:
1-[3,5-双(三氟甲基)苯基)-3-{(S)[(2S,4S,5R)-5-乙基-1-氮杂-二环[2.2.2]辛-2-基]-(6-甲氧基-4-喹啉基)甲基}硫脲, epi-N-二氢喹啉基-N′-双(3,5-三氟甲基)苯硫脲
经验公式（希尔记法）:
C29H30F6N4OS
推荐产品
![N-[3,5-双(三氟甲基)苯基]-N′-[(8a,9S)-6′-甲氧基-9-金鸡宁]硫脲 90%](/deepweb/assets/sigmaaldrich/product/structures/634/236/e688c89f-a93b-4698-a6fc-48e479a875cb/640/e688c89f-a93b-4698-a6fc-48e479a875cb.png)
![1,3-双[3,5-双(三氟甲基)苯基]硫脲 95%](/deepweb/assets/sigmaaldrich/product/structures/191/427/0218c99c-65b9-4963-938c-c47a5790dfc5/640/0218c99c-65b9-4963-938c-c47a5790dfc5.png)
![(R)-N-[(1R,2R)-2-(3-(3,5-双(三氟甲基)苯基)脲基)环己基]-叔丁基亚磺酰胺 96%](/deepweb/assets/sigmaaldrich/product/structures/389/070/18847164-c6a7-4b4e-abcb-2dbc22493a2d/640/18847164-c6a7-4b4e-abcb-2dbc22493a2d.png)
![N-[(1R,2R)-2-(1-哌啶基）环己基]-N′-[4-（三氟甲基）苯基]四酰胺 95%](/deepweb/assets/sigmaaldrich/product/structures/238/480/7149c9c0-8769-418a-a96c-77c15dd50cd0/640/7149c9c0-8769-418a-a96c-77c15dd50cd0.png)
![(S)-2-[[3,5-双(三氟甲基)苯基]硫脲基]-N-苄基-N,3,3-三甲基丁酰胺 97%](/deepweb/assets/sigmaaldrich/product/structures/373/888/118b46f2-6c2e-4a87-8266-c4dbcd5db51f/640/118b46f2-6c2e-4a87-8266-c4dbcd5db51f.png)
![N-[3,5-双(三氟甲基)苯基]-N′-[(9R)-6′-甲氧基-9-金鸡宁]硫脲 ≥90.0%](/deepweb/assets/sigmaaldrich/product/structures/406/654/594d25ee-3436-4bf4-ae14-d9b677568d2a/640/594d25ee-3436-4bf4-ae14-d9b677568d2a.png)
![1-[3,5-bis(trifluoromethyl)phenyl]-3-[(1R,2R)-(-)-2-(dimethylamino)cyclohexyl]thiourea AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/236/021/d944889d-2233-4700-9f2c-caa3652d0124/640/d944889d-2233-4700-9f2c-caa3652d0124.png)
![1-[3,5-Bis(trifluoromethyl)phenyl]-3-[(1R,2R)-(−)-2-(dimethylamino)cyclohexyl]thiourea](/deepweb/assets/sigmaaldrich/product/structures/384/772/d336462c-f438-446d-be0c-4064705213cc/640/d336462c-f438-446d-be0c-4064705213cc.png)
质量水平
检测方案
≥89.0% (HPLC)
90%
形式
lumps
旋光性
[α]/D -107.0±5.0°, c = 1 in chloroform
SMILES字符串
CC[C@H]1CN2CCC1CC2[C@@H](NC(=S)Nc3cc(cc(c3)C(F)(F)F)C(F)(F)F)c4ccnc5ccc(OC)cc45
InChI
1S/C29H30F6N4OS/c1-3-16-15-39-9-7-17(16)10-25(39)26(22-6-8-36-24-5-4-21(40-2)14-23(22)24)38-27(41)37-20-12-18(28(30,31)32)11-19(13-20)29(33,34)35/h4-6,8,11-14,16-17,25-26H,3,7,9-10,15H2,1-2H3,(H2,37,38,41)/t16-,17-,25-,26-/m0/s1
InChI key
KBYUJTLQXUVPQI-FRSFCCSCSA-N
应用
采用双官能金鸡纳有机催化剂，进行硝基甲烷的高度对映选择性共轭加成反应，生成查耳酮
包装
Bottomless glass bottle. Contents are inside inserted fused cone.
警示用语：
Danger
危险声明
预防措施声明
危险分类
Acute Tox. 3 Oral
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
新产品
Urea- and thiourea-substituted cinchona alkaloid derivatives as highly efficient bifunctional organocatalysts for the asymmetric addition of malonate to nitroalkenes: inversion of configuration at C9 dramatically improves catalyst performance.
Séamus H McCooey et al.
Angewandte Chemie (International ed. in English), 44(39), 6367-6370 (2005-09-02)
Benedek Vakulya et al.
Organic letters, 7(10), 1967-1969 (2005-05-07)
Cinchona alkaloid-derived chiral bifunctional thiourea organocatalysts were synthesized and applied in the Michael addition between nitromethane and chalcones with high ee and chemical yields.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门