89941-77-5

Basic information

• Product Name: Methyl 2-methoxytetrahydro-3-furoate
• Synonyms: Methyl 2-methoxytetrahydro-3-furoate;3-Furancarboxylicacid,tetrahydro-2-methoxy-,methylester(9CI);Alkyl-2-alkoxytetrahydro-3-furoate
• CAS NO: 89941-77-5
• Molecular Formula: C₇H₁₂O₄
• Molecular Weight: 160.16778
• Product Categories: CARBOXYLICESTER
• Mol File: 89941-77-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Methyl 2-methoxytetrahydro-3-furoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-methoxytetrahydro-3-furoate(89941-77-5)
• EPA Substance Registry System: Methyl 2-methoxytetrahydro-3-furoate(89941-77-5)

Safety Data

• Hazardous Substances Data: 89941-77-5(Hazardous Substances Data)

Usage

General Description

Methyl 2-methoxytetrahydro-3-furoate is a chemical compound with the molecular formula C7H12O4. It is a synthetic ester that is commonly used as a flavoring agent and fragrance ingredient in various consumer products. The compound has a sweet, fruity odor and is often utilized in the production of perfumes, soaps, and cosmetics. Additionally, it is frequently employed in the food industry to enhance the flavor of products such as beverages and confectionery items. Methyl 2-methoxytetrahydro-3-furoate is known for its stability, solubility, and low volatility, making it a versatile ingredient in the manufacturing of scented and flavored goods.

Upstream product

• 96-48-0 4-butanolide 
• 109-94-4 formic acid ethyl ester 
• 67-56-1 methanol 
• 107-31-3 Methyl formate 
• 61541-20-6 methyl 4-hydroxy-2-methylenebutanoate 
• 83124-80-5 3-trichloroacetyl-4,5-dihydrofuran 
• 127915-15-5 2-oxotetrahydrofuran-3-carboxylic acid methyl ester 
• 7647-01-0 hydrogenchloride 
• 53855-26-8 2-formyl-γ-butyrolactone 

Downstream Products

• 53750-81-5 4,5-dihydro-furan-3-carboxylic acid methyl ester 
• 25714-71-0 4-hydroxybutyraldehyde 
• 1708-33-4 4-hydroxy-butyraldehyde-(2,4-dinitro-phenylhydrazone) 
• 206860-63-1 C₁₇H₂₇Cl₂N₂O₄P 
• 98021-62-6 4,5-dihydrofuran-3-carboxylic acid 
• 65038-86-0 4,5-dihydro-furan-3-carboxylic acid p-toluidide 
• 933770-71-9 α-benzyloxymethyl-γ-lactone 

Relevant articles and documents

HETEROCYCLIC AMIDES AS ROCK INHIBITORS

The present invention relates to new kinase inhibitors of formula (I), more specifically ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In particular, the present invention relates to new ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In addition, the invention relates to methods of treatment and use of said compounds in the manufacture of a medicament for the application to a number of therapeutic indications including sexual dysfunction, inflammatory diseases, ophthalmic diseases and Respiratory diseases.

Haloacetylated Enol Ethers: 4. Synthesis of 4-Trihalomethyl-2-methylthiopyrimidines

The synthesis of a series of 5- and 6-substituted 4-trihalomethyl-2-methylthiopyrimidines, prepared from the cyclocondensation reaction of β-alkoxyvinyl trichloromethyl ketones with 2-methyl-2-thiopseudourea sulfate, are reported.A systematic study to find the best reation conditions werre carried out.

STEREOSELECTIVE SYNTHESES OF 2-SUBSTITUTED PERHYDROFUROFURANS

New reagents for the stereoselective synthesis of 2-substituted perhydrofurofurans are described.In the successful approach towards the latter compounds, the key steps were the addition of a monolithio-2α-methoxy-3β-perhydrofuran to an aldehyde and a dilithio-2α-methoxy-3β-perhydrofuran to a carboxyl derivative, respectively.The structures and conformations of the 2-tert-butyl- and 2-isopropylperhydrofurofurans were examined by means of (1)H-NMR double resonance and the 2D-NOE spectroscopy.