68634-03-7

Basic information

• Product Name: 6-METHOXYCARBONYL-1-INDANONE
• Synonyms: Methyl 1-oxoindan-6-carboxylate;3-Oxo-indan-5-carboxylic acid methyl ester;6-METHOXYCARBONYL-1-INDANONE;Methyl 3-oxo-2,3-dihydro-1H-indene-5-carboxylate;1H-INDENE-5-CARBOXYLIC ACID,2,3-DIHYDRO-3-OXO-, METHYL ESTER;6-Methoxycarbonyl-1-Indanone(WX618394)
• CAS NO: 68634-03-7
• Molecular Formula: C₁₁H₁₀O₃
• Molecular Weight: 190.1953
• Mol File: 68634-03-7.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: 6-METHOXYCARBONYL-1-INDANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-METHOXYCARBONYL-1-INDANONE(68634-03-7)
• EPA Substance Registry System: 6-METHOXYCARBONYL-1-INDANONE(68634-03-7)

Safety Data

• Hazardous Substances Data: 68634-03-7(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
6-METHOXYCARBONYL-1-INDANONE is used as a reactant in organic synthesis for [application reason] the synthesis of various organic compounds. Its reactivity and functional groups make it a versatile building block for creating a wide range of molecules with different applications.
Used in Plant Growth Regulation:
6-METHOXYCARBONYL-1-INDANONE is used as a plant growth regulating compound for [application reason] controlling and modifying the growth and development of plants. It can be employed in the agricultural industry to enhance crop yield, improve resistance to environmental stressors, and regulate the maturation process.
If there are different applications in different industries, they are listed separately:
Used in Pharmaceutical Industry:
6-METHOXYCARBONYL-1-INDANONE is used as an intermediate in the synthesis of pharmaceutical compounds for [application reason] its potential to be incorporated into drug molecules targeting various diseases and conditions.
Used in Chemical Research:
6-METHOXYCARBONYL-1-INDANONE is used as a research compound for [application reason] studying its chemical properties, reactivity, and potential applications in the development of new materials and chemicals.

Upstream product

• 67-56-1 methanol 
• 60031-08-5 Indan-1-one-6-carboxylic acid 
• 86031-43-8 methyl 5-indanecarboxylate 
• 65898-38-6 indan-5-carboxylic acid 
• 15497-40-2 2,3-dihydroindene-5-carbonyl chloride 
• 858124-35-3 4-bromo-3-formyl-benzoic acid methyl ester 
• 1095432-84-0 2-bromo-5-(methoxycarbonyl)phenylmethylene diacetate 
• 1313762-39-8 3-formyl-4-vinylbenzoic acid methyl ester 
• 148547-19-7 4-Bromo-3-methylbenzoic acid methyl ester 
• 38628-51-2 3-(4-carboxyphenyl)propionic acid 
• 4228-10-8 1-indan-5-yl-ethanone 
• 496-11-7 INDANE 

Downstream Products

• 178208-96-3 Methyl 2-[2-(N-Benzyloxycarbonylpiperidin-4-yl)ethyl]indan-1-one-6-carboxylate 

Relevant articles and documents

Ratiometric O2 sensing based on selective self-sensitized photooxidation of donor-acceptor fluorophores

We report a series of organic fluorophores that undergo selective self-sensitized photooxidation upon light irradiation in air accompanied by a change of fluorescence from yellow to blue on the seconds timescale. The distinct emission changes allow the ratiometric quantitation of O2 concentration.

AMINO-PYRIDINE-CONTAINING SPLEEN TYROSINE KINASE (SYK) INHIBITORS

The invention provides certain amino-pyridine-containing compounds of the Formula (I) or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, and n are as defined herein. The invention also provides pharmaceutical compositions comprising such compounds, and methods of using the compounds for treating diseases or conditions mediated by Spleen Tyrosine Kinase (Syk) kinase.

Substituted Benzamide Compounds

Substituted benzamide compounds corresponding to formula (I) in which R5, R6, R7, R8, a, b, c, d, t, D and X have defined meanings, a process for their preparation, pharmaceutical compositions comprising such compounds, and a method of using such compounds to treat pain and other conditions mediated at least in part via the bradykinin 1 receptor.

Inter- and intramolecular hydroacylation of alkenes employing a bifunctional catalyst system

Based on a conceptually innovative bifunctional P,N ligand, an efficient protocol for the rhodium-catalyzed inter- and intramolecular hydroacylation of alkenes has been developed.

Substituted Spiro-amide Compounds

Substituted spiro-amide compounds corresponding to formula I in which R5 through R8, D, X, Y and Z have defined meanings, processes for preparing such spiro-amide compounds, pharmaceutical compositions containing such compounds, and methods of using such spiro-amide compounds for treating and/or inhibiting disorders or disease states mediated at least in part by the bradykinin 1 receptor.

Syntheses of compounds active toward glutamate receptors: I. New preparative synthesis of aminoindandicarboxylic acid (AIDA)

A preparative procedure has been developed for the synhtesis of 1-aminoindan-1,5-dicarboxylic acid which is a new group I metabotropic glutamate receptor antagonist.