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About This Item
Empirical Formula (Hill Notation):
C15H20Cl2N2O3
CAS Number:
Molecular Weight:
347.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Quality Level
assay
97%
mp
122-126 °C
functional group
carboxylic acid, chloro, phenyl
SMILES string
OC(=O)C(Cl)Cl.CN1C(=O)[C@H](Cc2ccccc2)NC1(C)C
InChI
1S/C13H18N2O.C2H2Cl2O2/c1-13(2)14-11(12(16)15(13)3)9-10-7-5-4-6-8-10;3-1(4)2(5)6/h4-8,11,14H,9H2,1-3H3;1H,(H,5,6)/t11-;/m0./s1
InChI key
YZRAPAXOLQHZSE-MERQFXBCSA-N
Application
Utilized in the first example of organocatalytic enantioselective α-fluorination of aldehydes.
Legal Information
U.S. Pat. 6,369,243 and related patents apply. For research purposes only.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Articles
Discover Professor David MacMillan's groundbreaking metal-free asymmetric catalysis using imidazolidinone-based organocatalysts for versatile transformations.
Teresa D Beeson et al.
Journal of the American Chemical Society, 127(24), 8826-8828 (2005-06-16)
The first direct enantioselective catalytic alpha-fluorination of aldehydes has been accomplished. The use of enamine catalysis has provided a new organocatalytic strategy for the enantioselective fluorination of aldehydes to generate alpha-fluoro aldehydes, an important chiral synthon for medicinal agent synthesis.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 663085-2G | 04061833549148 |
| 663085-500MG | 04061838128607 |

