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Merck
CN

156728

6-Methyl-4-chromanone

97%

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About This Item

Empirical Formula (Hill Notation):
C10H10O2
CAS Number:
Molecular Weight:
162.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
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assay

97%

form

solid

bp

141-143 °C/13.5 mmHg (lit.)

mp

31-35 °C (lit.)

density

1.071 g/mL at 25 °C (lit.)

functional group

ketone

SMILES string

Cc1ccc2OCCC(=O)c2c1

InChI

1S/C10H10O2/c1-7-2-3-10-8(6-7)9(11)4-5-12-10/h2-3,6H,4-5H2,1H3

InChI key

RJHXEPLSJAVTFW-UHFFFAOYSA-N

Application

The product has been used as a substrate for carbonyl reductase from Sporobolomyces salmonicolor, wherein it was reduced to the corresponding (R)-chiral alcohol. It has also been used as a substrate for the enantioselective reduction by 3 biocatalysts, namely, Didymosphaeria igniaria, Coryneum betulinum and Chaetomium sp.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Enantioselective reduction of 4-chromanone and its derivatives by selected filamentous fungi.
Janeczko T, et al.
Journal of Molecular Catalysis. B, Enzymatic, 97, 278-282 (2013)
Dunming Zhu et al.
Organic & biomolecular chemistry, 4(14), 2690-2695 (2006-07-11)
In our effort to search for effective carbonyl reductases, the activity and enantioselectivity of a carbonyl reductase from Sporobolomyces salmonicolor have been evaluated toward the reduction of a variety of ketones. This carbonyl reductase (SSCR) reduces a broad spectrum of



Global Trade Item Number

SKUGTIN
156728-5G04061838089847