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Merck
CN

804576

Sigma-Aldrich

(1E)-4-Hydroxy-1-mesityl-4-methylpent-1-en-3-one

Synonym(s):

Bode Hydroxamic Acid

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About This Item

Empirical Formula (Hill Notation):
C15H20O2
CAS Number:
1346681-71-7
Molecular Weight:
232.32
UNSPSC Code:
12352000
PubChem Substance ID:
329768883
NACRES:
NA.22

Key Documents

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form

crystals

mp

75-77 °C

functional group

hydroxyl
ketone

SMILES string

O=C(C(C)(C)O)/C=C/C1=C(C)C=C(C)C=C1C

InChI

1S/C15H20O2/c1-10-8-11(2)13(12(3)9-10)6-7-14(16)15(4,5)17/h6-9,17H,1-5H3/b7-6+

InChI key

MZEPKOZFBZWACD-VOTSOKGWSA-N

Application

The following hydroxamic acid was shown by Bode and coworkers to assist in the kinetic resolution of cyclic amines through acylation of one enantiomer, which can be controlled using either the (R,S)- or (S,R)-Bode Kinetic Resolution Catalyst, both of which are also available through Sigma-Aldrich. 

Other Notes

Catalytic Kinetic Resolution of Cyclic Secondary Amines

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Related Content

Bode Group – Prof. Product Portal

Bode Group creates N-mesityl-NHC catalysts for enantioselective annulations and SnAP reagents for one-pot aldehyde conversion into N-heterocycles.

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