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615-10-1

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615-10-1 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 615-10-1 differently. You can refer to the following data:
1. Colorless, fragrant liquid; becomes yel- low in light. Practically insol- uble in water; soluble in alcohol and ether. Com- bustible.
2. Propyl 2-furoate has a peculiar, sweet–oily, herbaceous–earthy odor.

Uses

Flavoring.

Check Digit Verification of cas no

The CAS Registry Mumber 615-10-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 615-10:
(5*6)+(4*1)+(3*5)+(2*1)+(1*0)=51
51 % 10 = 1
So 615-10-1 is a valid CAS Registry Number.

615-10-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Propyl 2-Furancarboxylate

1.2 Other means of identification

Product number -
Other names 2-Furancarboxylic acid, propyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:615-10-1 SDS

615-10-1Downstream Products

615-10-1Relevant articles and documents

Selective transformation of renewable furfural catalyzed by diverse active species derived from 2D co-based metal-organic frameworks

Ning, Liangmin,Liao, Shengyun,Liu, Xuguang,Yu, Linhao,Zhuang, Xuli,Tong, Xinli

, p. 480 - 490 (2017)

We report a facile method for gaining two different types of highly active species from the same 2D Co-based MOFs, which can effectively catalyze the selective transformation of biomass-derived furfural (FUR) in alcohols. Removal of the coordinated water molecules from the Co-based MOFs at 300?°C creates the open metal centers as catalytic active species (designated as ACS-I catalyst). Increasing the pyrolysis temperature to 700?°C, the derived multi-element carbon-matrix nanocomposite from the MOFs (designated as ACS-II catalyst) also shows highly catalytic performance. Both catalyst ACS-I and ACS-II exhibit high reactivity (84.9% conv.) and excellent selectivity (ca. 99.0%) in the oxidative condensation of FUR with n-propanol to produce 3-(furan-2-yl-)-2-methylacrylaldehyde (2) in the presence of molecular oxygen. The particular evidence for the role of metal Co centers in ACS-I and ACS-II is originated from the catalyst characterization and control experiments, in which Ni-I and Ni-II catalysts derived from isomorphrous 2D Ni-based MOFs show no catalytic activity on the transformation of FUR under the similar conditions.

Preparation method of furfuryl ester (by machine translation)

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Paragraph 0023-0025; 0057-0059, (2020/06/22)

The preparation method comprises the following steps: uniformly mixing furfural, an oxidation esterification catalyst, a cocatalyst and a solvent, and reacting under the condition of an oxygen source for a period of time under a certain temperature and pressure to obtain the furfuryl ester. The method is high in selectivity, few in byproducts and mild in reaction condition, and has a certain industrial application prospect. (by machine translation)

Zinc-Catalyzed Esterification of N-β-Hydroxyethylamides: Removal of Directing Groups under Mild Conditions

Nishii, Yuji,Hirai, Takahiro,Fernandez, Sarah,Knochel, Paul,Mashima, Kazushi

, p. 5010 - 5014 (2017/09/21)

Amide transformations involving C–N bond cleavage are recognized as difficult reactions owing to the inert nature of amides resulting from resonance. Accordingly, a strong inductive effect and geometrical distortion reasonably decrease the resonance stabilization to attenuate the C–N linkage. Although the conversion of such activated amides has been studied intensively, reaction systems for “unactivated” amides are underdeveloped. We herein report that a zinc(II) trifluoromethanesulfonate [Zn(OTf)2] catalyst achieves the esterification of a wide range of unactivated tertiary amides with the assistance of intramolecular acyl rearrangement. The reaction was applied to the one-pot removal of various amide-based directing groups under mild reaction conditions to afford the corresponding esters in high yields.

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