375825-11-9

Basic information

• Product Name: 2-Furancarboxylicacid,tetrahydro-,ethylester,(2R)-(9CI)
• Synonyms: 2-Furancarboxylicacid,tetrahydro-,ethylester,(2R)-(9CI)
• CAS NO: 375825-11-9
• Molecular Formula: C7H12O3
• Molecular Weight: 144.17
• Product Categories: CARBOXYLICESTER
• Mol File: 375825-11-9.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 180.8±23.0 °C(Predicted)
• Appearance: /
• Density: 1.076±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Furancarboxylicacid,tetrahydro-,ethylester,(2R)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furancarboxylicacid,tetrahydro-,ethylester,(2R)-(9CI)(375825-11-9)
• EPA Substance Registry System: 2-Furancarboxylicacid,tetrahydro-,ethylester,(2R)-(9CI)(375825-11-9)

Safety Data

• Hazardous Substances Data: 375825-11-9(Hazardous Substances Data)

Upstream product

• 88-14-2 2-furanoic acid 
• 64-17-5 ethanol 
• 75-07-0 acetaldehyde 
• 614-99-3 Ethyl 2-furoate 
• 503-30-0 trimethylene oxide 
• 623-73-4 diazoacetic acid ethyl ester 
• 67-56-1 methanol 
• 52449-98-6 tetrahydrofuran-2-carbonyl chloride 
• 16874-33-2 tetrahydro-2-furancarboxylic acid 
• 16874-34-3 ethyl tetrahydrofurancarboxylate 
• 87392-05-0 (R)-tetrahydro-2-furoic acid 

Downstream Products

• 887411-85-0 ethyl 3-oxo-3-(tetrahydrofuran-2-yl)propanoate 
• 103329-62-0 6-methoxy-5,7,8-triphenyl-1,2,3,4-tetrahydro-[1]naphthoic acid 
• 59293-11-7 tetrahydrofuran-2-carboxylic acid hydrazide 
• 91470-28-9 tetrahydrofuran-2-carboxamide 
• 1730-58-1 (5-ethyl-5,6,7,8-tetrahydro-[2]naphthyl)-methyl ether 
• 108-95-2 phenol 
• 1028843-21-1 3-(tetrahydrofuran-2-yl)-1H-pyrazol-5-amine 

Relevant articles and documents

Preparation method of tetrahydrofuranacetic acid and ester compounds thereof

The invention provides a preparation method of tetrahydrofuranacetic acid and ester compounds thereof. The preparation method comprises the following steps: in a proper solvent, in a reducing atmosphere and under the action of a hydrogenation catalyst, carrying out a reduction reaction on furanacetic acid and ester compounds thereof under the conditions that a pressure is 0.1-10MPa and a temperature is 30-250 DEG C for 0.1-72 hours, separating out the catalyst, and distilling out the solvent to obtain the target products, namely tetrahydrofuranacetic acid and the ester compounds thereof. Under relatively mild and environment-friendly conditions, efficient conversion of bio-based furanacetic acid and esters thereof is achieved, industrial production of the reaction is facilitated, platform molecules can be converted into various important intermediates or terminal products through chemical catalysis upgrading to replace existing petrochemical products, dependence on fossil resources is reduced, and the application range of biomass is expanded.

TETRAHYDROFURAN DERIVATIVES AS FRAGRANCES

What is proposed are specific tetrahydrofuran derivatives of the formula (I), fragrance and aroma substance mixtures comprising these tetrahydrofuran derivatives, their use in fragrance or aroma substance (mixture) and corresponding perfumed products.

A selenide-based approach to photochemical cleavage of peptide and protein backbones at engineered backbone esters

(Chemical Equation Presented) A strategy for photochemical cleavage of peptide and protein backbones is described, which is based on a selenide-mediated cleavage of a backbone ester moiety. Studies in model systems establish the viability of the chemistry