ChemicalBook Product Catalog Chemical Reagents Organic reagents Aromatic ketones 6-Methoxy-1H-indanone

6-Methoxy-1H-indanone

6-Methoxy-1H-indanone Basic information
Product Name:6-Methoxy-1H-indanone
Synonyms:6-METHOXY-INDAN-1-ONE;6-METHOXY-1H-INDANONE;6-METHOXY-1-INDANONE;6-METHOXY-1-INDANONE, 97+%;6-Methoxy-I-indanone;6-Methoxy-1-indenone;6-METHOXY INDANONE;2,3-Dihydro-6-methoxy-1H-inden-1-one
CAS:13623-25-1
MF:C10H10O2
MW:162.19
EINECS:603-948-9
Product Categories:Indane/Indanone and Derivatives;indanone;Aromatics Compounds;Aromatics;C10;Carbonyl Compounds;Ketones
Mol File:13623-25-1.mol
6-Methoxy-1H-indanone Structure
6-Methoxy-1H-indanone Chemical Properties
Melting point 105-109 °C (lit.)
Boiling point 228.88°C (rough estimate)
density 1.0281 (rough estimate)
refractive index 1.6000 (estimate)
storage temp. Sealed in dry,Room Temperature
form Fine Crystalline Powder
color White to yellow
BRN 1238602
InChIKeyUJGDLLGKMWVCPT-UHFFFAOYSA-N
CAS DataBase Reference13623-25-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 22-24/25-36/37-36-26
WGK Germany 3
HS Code 29145090
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
6-Methoxy-1H-indanone Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
UsesIndanone derivative as a1-adrenoceptor antagonist.
UsesIndanone derivative as α1-adrenoceptor antagonist.
Uses6-Methoxy-1-indanone was used in the synthesis of 5-methoxyninhydrin (2,2-dihydroxy-5-methoxy-1,3-indanedione).
Synthesis Reference(s)Journal of the American Chemical Society, 71, p. 1092, 1949 DOI: 10.1021/ja01171a092
Purification MethodsCrystallise it from MeOH, then sublime it at high vacuum. [Beilstein 8 IV 894.]
6-Methoxy-1H-indanone Preparation Products And Raw materials
Preparation ProductsRamelteon-->1H-INDEN-1-ONE, 6-METHOXY--->1H-Indene, 5-methoxy-3-methyl--->1H-Indene-3-ethanamine, 5-methoxy--->5-methoxy-3,3-dimethylindane-->3-CHLORO-7-METHOXYISOQUINOLINE
Donepezil 5-METHOXYNINHYDRIN MONOHYDRATE 2-((4-(DIFLUOROMETHOXY)PHENYL)METHYLENE)-5,6-DIMETHOXYINDAN-1-ONE 6-Methoxy-1H-indanone DONEPEZIL HYDROCHLORIDE 5,6-DIMETHOXY-2-((4-METHOXYPHENYL)METHYLENE)INDAN-1-ONE 4-Bromo-6,7-dimethoxyindanone 1H-Indene-4-carboxylic acid, 2,3-dihydro-6,7-dimethoxy-1-oxo- Flosulide 5,6-Dimethoxy-1-indanone 2,2-DIHYDROXY-5-METHOXY-1,3-INDANDIONE HYDRATE 5,6-DIMETHOXY-2-(3-PHENYLPROP-2-ENYLIDENE)INDAN-1-ONE 2-((4-DIMETHYLAMINOPHENYL)METHYLENE)-5,6-DIMETHOXYINDAN-1-ONE 5-METHOXY-1-INDANONE-3-ACETIC ACID 5,6-DIMETHOXY-2-((3-PHENOXYPHENYL)METHYLENE)INDAN-1-ONE (+)-Fumariline 4,5,6-TRIMETHOXY-INDANONE 2-BROMO-2,3-DIHYDRO-5,6-DIMETHOXY-1H-INDEN-1-ONE
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