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14313-09-8

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14313-09-8 Usage

Uses

3-Acetylfuran is used as the primary and secondary intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 14313-09-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,1 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14313-09:
(7*1)+(6*4)+(5*3)+(4*1)+(3*3)+(2*0)+(1*9)=68
68 % 10 = 8
So 14313-09-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O2/c1-5(7)6-2-3-8-4-6/h2-4H,1H3

14313-09-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H34071)  3-Acetylfuran, 97%   

  • 14313-09-8

  • 250mg

  • 669.0CNY

  • Detail
  • Alfa Aesar

  • (H34071)  3-Acetylfuran, 97%   

  • 14313-09-8

  • 1g

  • 1862.0CNY

  • Detail

14313-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-Furyl)-1-ethanone

1.2 Other means of identification

Product number -
Other names 3-Acetylfuran

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:14313-09-8 SDS

14313-09-8Relevant articles and documents

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Ohlsen,Turner

, p. 1632 (1971)

-

A mild, efficient approach to 3-acylfurans: A short synthesis of perilla ketone

Bailey

, p. 242 - 243 (1991)

Several 3-acylfurans 3 were prepared in excellent yield using a one-pot procedure involving the palladium-catalyzed cross-coupling of commercially available acid chlorides with tributyl(3-furyl)-stannane 2 at room temperature.

Synthesis, structure and pyrolysis of stabilised phosphonium ylides containing saturated oxygen heterocycles

Aitken, R. Alan,Karodia, Nazira,McCarron, Hollie B.,Rouxel, Cécile,Sahabo, Nina,Slawin, Alexandra M. Z.

, p. 1794 - 1804 (2016/02/10)

A range of twelve stabilised phosphonium ylides containing tetrahydrofuran, tetrahydropyran or 2,2-dimethyl-1,3-dioxolane rings have been prepared and fully characterised, including one X-ray structure determination of each type. The X-ray structures confirm the P=C and C=O functions to be syn and all the compounds undergo thermal extrusion of Ph3PO to give the corresponding alkynes. In some cases there is also competing loss of Ph3P to give different carbene-derived products and evidence has been obtained for the generation of 2-phenyloxete in this way. Raising the pyrolysis temperature leads in several cases to new secondary reactions of the alkyne products involving a sequence of alkyne to vinylidene isomerisation, intramolecular CH insertion, and retro Diels Alder reaction.

Synthesis of industrially important aromatic and heterocyclic ketones using hierarchical ZSM-5 and Beta zeolites

Kore, Rajkumar,Srivastava, Rajendra,Satpati, Biswarup

, p. 129 - 141 (2015/09/28)

Hierarchical ZSM-5 and Beta zeolites were investigated in the synthesis of wide range of industrially important aromatic/heterocyclic ketones by Friedel-Crafts acylation and benzoylation reactions. For comparative study, conventional ZSM-5 and Beta, and amorphous mesoporous Al-MCM-41 were investigated. Hierarchical zeolites were prepared by multi-ammonium structure directing agents whereas conventional zeolites were prepared by mono-ammonium structure directing agents. Among the catalysts investigated in this study, hierarchical Beta exhibited the highest reactant conversion in the acylation and benzoylation reactions. In this study, the systematic assessment of the catalytic activity of acid catalysts for wide range of aromatic and heterocyclic compounds is shown under one umbrella. To the best of our knowledge, these reactions over hierarchical zeolites (ZSM-5 and Beta) are reported here for the first time. Structure activity relationship is explained based on the physico-chemical properties, molecular size, reactivity of reactants, and reaction mechanism. Catalysts can be easily recovered and reused with negligible loss in the catalytic activity.

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