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Merck
CN

680826

Sigma-Aldrich

(–)-(S)-N-((R)-3,3-Dimethylbutan-2-yl)-3,3-dimethyl-2-((1-methyl-1H-imidazol-2-yl)methylamino)butanamide

97%

Synonym(s):

Hoveyda-Snapper Desymmetrization Catalyst

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About This Item

Empirical Formula (Hill Notation):
C17H32N4O
CAS Number:
Molecular Weight:
308.46
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
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Assay

97%

form

solid

optical activity

[α]22/D -79°, c = 1 in chloroform

mp

130-134 °C

SMILES string

C[C@@H](NC(=O)[C@@H](NCc1nccn1C)C(C)(C)C)C(C)(C)C

InChI

1S/C17H32N4O/c1-12(16(2,3)4)20-15(22)14(17(5,6)7)19-11-13-18-9-10-21(13)8/h9-10,12,14,19H,11H2,1-8H3,(H,20,22)/t12-,14-/m1/s1

InChI key

QOCLPFRRAGRCEM-TZMCWYRMSA-N

Application

Useful organocatalyst in the desymmetrization of meso diols.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Yu Zhao et al.
Nature, 443(7107), 67-70 (2006-09-08)
Reliable, selective and environmentally friendly chemical transformations are crucial to the development of new therapeutics and the design of novel materials. Chiral catalysts that can be easily prepared and used to obtain organic molecules of high enantiomeric purity are critical

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