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5-acetyldihydro-2-hydroxy-2,5-dimethylfuran-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29549-78-8

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29549-78-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29549-78-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,5,4 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 29549-78:
(7*2)+(6*9)+(5*5)+(4*4)+(3*9)+(2*7)+(1*8)=158
158 % 10 = 8
So 29549-78-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O4/c1-5(9)7(2)4-6(10)8(3,11)12-7/h11H,4H2,1-3H3

29549-78-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-acetyl-2-hydroxy-2,5-dimethyloxolan-3-one

1.2 Other means of identification

Product number -
Other names EINECS 249-691-2

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:29549-78-8 SDS

29549-78-8Downstream Products

29549-78-8Relevant academic research and scientific papers

Thiazolium-functionalized polystyrene monolithic microreactors for continuous-flow umpolung catalysis

Bortolini, Olga,Cavazzini, Alberto,Dambruoso, Paolo,Giovannini, Pier Paolo,Caciolli, Lorenzo,Massi, Alessandro,Pacifico, Salvatore,Ragno, Daniele

, p. 2981 - 2992 (2013/10/08)

Thiazolium salt pre-catalysts have been immobilized on silica and monolithic polystyrene and their activity was tested under batch conditions in three model umpolung reactions, namely the benzoin condensation of benzaldehyde, the acyloin-type condensation of biacetyl, and the Stetter reaction of biacetyl with trans-chalcone. A prerequisite of the study has been the utilization of environmentally benign water and ethanol solvents. After having established the higher performance of polystyrene monolithic thiazolium carbene catalysts, their effectiveness has been tested under the flow regime by fabricating the corresponding monolithic microreactors (pressure-resistant stainless-steel columns). Importantly, it has been demonstrated by a brief substrate scope study that the polymeric matrix and the continuous flow regime synergistically contribute to preserve the activity of the carbene catalysts over time, thus permitting the long-term operation (up to 7 days) of the prepared monolithic reactors for the production of valuable compounds via the umpolung strategy.

THE STEREOSTRUCTURE OF TWO TRIMERS OF BIACETYL

Poje, M.,Perina, I.,Vickovic, I.,Bruvo, M.

, p. 1985 - 1988 (2007/10/02)

Structures of two trimers of biacetyl were determined on the basis of chemical and spectroscopic evidence and the single-crystal X-ray analysis.The compounds are shown to be exo-3,endo-7-diacetyl-1-hydroxy-endo-3,5,exo-7-trimethyl-cis-2,4,6-trioxabicyclooctane (2) and 11-hydroxy-1,3,5,7,11-pentamethyl-cis-2,4,6,8-tetraoxatricyclo3,7>undecan-9-one (3).

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