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About This Item
Empirical Formula (Hill Notation):
C29H28F6N4OS
CAS Number:
Molecular Weight:
594.61
UNSPSC Code:
12352005
PubChem Substance ID:
MDL number:
assay
≥90.0% (HPLC), ≥90.0%
form
lumps
functional group
amine, fluoro, thiourea
SMILES string
COc1ccc2nccc([C@@H](NC(=S)Nc3cc(cc(c3)C(F)(F)F)C(F)(F)F)C4CC5CCN4C[C@@H]5C=C)c2c1
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
InChI key
IQMKPBFOEWWDIQ-ZRJNXXGPSA-N
General description
The product is a cinchona-alkaloid-derived, bifunctional catalyst containing a thiourea group at position 9.
Application
N-[3,5-Bis(trifluoromethyl)phenyl]-N′-[(9R)-6′-methoxy-9-cinchonanyl]thiourea may be used to catalyze the formation of optically active Mannich adducts from stable N-carbamate amido sulfones via enantioselective Mannich reaction.
Highly enantioselective conjugate addition of nitromethane to chalcones using bifunctional cinchona organocatalysts
Features and Benefits
N-[3,5-Bis(trifluoromethyl)phenyl]-N′-[(9R)-6′-methoxy-9-cinchonanyl]thiourea as an organocatalyst has the following advantages over transition-metal catalysis:
- Lower toxicity
- Lower costs
- Air and moisture stability for simple reaction setup
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Danger
hcodes
pcodes
Hazard Classifications
Acute Tox. 3 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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