Skip to Content
Merck
All Photos(2)

Documents

225282

Sigma-Aldrich

5-Methoxy-1-indanone-3-acetic acid

technical grade

Synonym(s):

6-Methoxy-3-oxo-1-indanacetic acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H12O4
CAS Number:
Molecular Weight:
220.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

form

powder

mp

139-144 °C (lit.)

solubility

chloroform: soluble 5%, clear, yellow-brown

SMILES string

COc1ccc2C(=O)CC(CC(O)=O)c2c1

InChI

1S/C12H12O4/c1-16-8-2-3-9-10(6-8)7(4-11(9)13)5-12(14)15/h2-3,6-7H,4-5H2,1H3,(H,14,15)

InChI key

QOTZOFGBBCMWEP-UHFFFAOYSA-N

General description

The 5-methoxy-1-indanone-3-acetic acid derivatives are potent inhibitors of chymotrypsin-like activity of the 20S proteasome.

Storage Class Code

11 - 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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

R T Lum et al.
Bioorganic & medicinal chemistry letters, 8(3), 209-214 (1999-01-01)
Potent inhibitors of the 20S proteasome that contain a novel indanone head group coupled to di and tripeptides are described. These compounds are the first proteasome inhibitors have demonstrated high selectivity for the chymotrypsin-like activity of the 20S proteasome.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service