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1-[3,5-bis(trifluoromethyl)phenyl]-3-[(R)-[(2R,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl](6-methoxyquinolin-4-yl)methyl]thiourea
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ChemBase ID:
141604
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Molecular Formular:
C29H28F6N4OS
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Molecular Mass:
594.6142392
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Monoisotopic Mass:
594.18880186
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SMILES and InChIs
SMILES:
COc1ccc2c(c1)c(ccn2)[C@H]([C@H]1C[C@@H]2CCN1C[C@@H]2C=C)NC(=S)Nc1cc(cc(c1)C(F)(F)F)C(F)(F)F
Canonical SMILES:
C=C[C@H]1CN2CC[C@H]1C[C@@H]2[C@@H](c1ccnc2c1cc(OC)cc2)NC(=S)Nc1cc(cc(c1)C(F)(F)F)C(F)(F)F
InChI:
InChI=1S/C29H28F6N4OS/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/h3-6,8,11-14,16-17,25-26H,1,7,9-10,15H2,2H3,(H2,37,38,41)/t16-,17-,25+,26+/m0/s1
InChIKey:
IQMKPBFOEWWDIQ-ZRJNXXGPSA-N
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Cite this record
CBID:141604 http://www.chembase.cn/molecule-141604.html
NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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1-[3,5-bis(trifluoromethyl)phenyl]-3-[(R)-[(2R,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl](6-methoxyquinolin-4-yl)methyl]thiourea
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IUPAC Traditional name
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1-[3,5-bis(trifluoromethyl)phenyl]-3-[(R)-[(2R,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl](6-methoxyquinolin-4-yl)methyl]thiourea
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Synonyms
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1-[3,5-Bis(trifluoromethyl)phenyl)-3-{(R)(6-methoxy-4-quinolinyl)-[(2R,4S,5R)-5-vinyl-1-aza-bicyclo[2.2.2]oct-2-yl]methyl}thiourea
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epi-N-Quinidyl-N′-bis(3,5-trifluoromethyl)phenylthiourea
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N-[3,5-Bis(trifluoromethyl)phenyl]-N′-[(9R)-6′-methoxy-9-cinchonanyl]thiourea
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1-[3,5-双(三氟甲基)苯基)-3-{(R)(6-甲氧基-4-喹啉基)-[(2R,4S,5R)-5-乙烯基-1-氮杂-二环[2.2.2]辛-2-基]甲基}硫脲
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epi-N-奎宁基-N′-双(3,5-三氟甲基)苯硫脲
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N-[3,5-双(三氟甲基)苯基]-N′-[(9R)-6′-甲氧基-9-金鸡宁]硫脲
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CAS Number
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MDL Number
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PubChem SID
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PubChem CID
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
Acid pKa
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9.287586
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H Acceptors
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3
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H Donor
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2
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LogD (pH = 5.5)
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3.8602545
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LogD (pH = 7.4)
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5.6135435
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Log P
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6.4556975
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Molar Refractivity
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150.865 cm3
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Polarizability
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56.79511 Å3
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Polar Surface Area
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49.42 Å2
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Rotatable Bonds
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8
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Lipinski's Rule of Five
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false
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DETAILS
DETAILS
Sigma Aldrich
Sigma Aldrich -
690600
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Application Highly enantioselective conjugate addition of nitromethane to chalcones using bifunctional cinchona organocatalysts1,2 Packaging 250 mg in glass bottle |
PATENTS
PATENTS
PubChem Patent
Google Patent