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183539

Sigma-Aldrich

5-Methoxy-1-indanone

98%

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About This Item

Empirical Formula (Hill Notation):
C10H10O2
CAS Number:
5111-70-6
Molecular Weight:
162.19
Beilstein:
1282137
EC Number:
225-838-6
MDL number:
MFCD00003789
UNSPSC Code:
12352100
PubChem Substance ID:
24851061
NACRES:
NA.22

Assay

98%

form

powder

mp

107-109 °C (lit.)

functional group

ketone

SMILES string

COc1ccc2C(=O)CCc2c1

InChI

1S/C10H10O2/c1-12-8-3-4-9-7(6-8)2-5-10(9)11/h3-4,6H,2,5H2,1H3

InChI key

QOPRWBRNMPANKN-UHFFFAOYSA-N

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General description

The cytotoxic potential of 5-methoxy-1-indanone was assessed[1].

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

183539-1G:
183539-500G:
183539-VAR:
183539-BULK:
183539-10G:
183539-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
STBG8274
STBB2136V
STBB2136
S13479
11601PH

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Tiffany J Somers-Edgar et al.
Anti-cancer drugs, 20(1), 33-40 (2008-10-03)
We postulated that methoxy-substituted cyclic compounds could inhibit estrogen receptor (ER) negative breast cancer growth in vitro. Therefore, this study assessed the cytotoxic potential of various methoxy-substituted cyclic compounds [7,8-dimethoxyflavone, 4-methoxyphenylacetic acid, 2-methoxyphenylacetic acid, 4-methoxybenzophenone, 5-methoxy-1-indanone, and coenzyme Q0 (CoQ0)]

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