392529
4-Methoxy-1-indanone
99%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
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:
99%
Quality Level
assay
99%
bp
115-120 °C/0.5 mmHg (lit.)
mp
105-107 °C (dec.) (lit.)
functional group
ketone
SMILES string
COc1cccc2C(=O)CCc12
InChI
1S/C10H10O2/c1-12-10-4-2-3-7-8(10)5-6-9(7)11/h2-4H,5-6H2,1H3
InChI key
BTYSYELHQDGJAB-UHFFFAOYSA-N
General description
4-Methoxy-1-indanone, a benzo-fused ketone is a 1-indanone derivative. Its synthesis has been reported.
Application
4-Methoxy-1-indanone is suitable for use in the comparative study of the effect of different substituents on various benzo-fused ketones on the reaction kinetics by studying the biocatalysed oxidation reaction.
It may be used in the following studies:
It may be used in the following studies:
- Synthesis of isomeric mixture of oximes.
- As a starting material in the synthesis of benzo-fused indolizidine and 4-methoxy-1-indanyl compound.
- Synthesis of 4-methoxy-5-nitro-1-indanone by nitration reaction.
- As one of the reactant in the synthesis of E-2-chloro-8-methyl-3-[(4′-methoxy-1′-indanoyl)-2′-methyliden]-quinoline (IQ), a quinoline derivative.
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
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
W H Pearson et al.
The Journal of organic chemistry, 65(21), 7158-7174 (2000-10-14)
The intramolecular capture of benzocyclobutyl, benzocyclopentyl, and benzocyclohexyl carbocations 7 by azides produces spirocyclic aminodiazonium ions 8, which undergo 1,2-C-to-N rearrangement with loss of dinitrogen to produce benzo-fused iminium ions resulting from either aryl (9) or alkyl (10) migration to
Enzymatic Baeyer-Villiger Oxidation of Benzo-Fused Ketones: Formation of Regiocomplementary Lactones.
Rioz-Martinez A, et al.
European Journal of Organic Chemistry, 2009(15), 2526-2532 (2009)
Beckmann rearrangements of 1-indanone oxime derivatives using aluminum chloride and mechanistic considerations.
Lee BS, et al.
Bull. Korean Chem. Soc., 21(9), 860-866 (2000)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 392529-1G | 04061831981551 |