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18545-28-3

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18545-28-3 Usage

General Description

3-oxopropyl acetate, also known as acetic acid, is a type of ester compound with the chemical formula C5H8O3. This organic compound is colorless and it has a sweet, fruity odor, but is considered harmful if swallowed, inhaled, or comes into contact with the skin or eyes. It may also cause respiratory irritation. It is generally used in organic synthesis and fragrances due to its odor. Its other names include 3-keto propyl acetate and methyl acetylacetate. It is a derivative of acetic acid, one of the simplest carboxylic acids. It plays a significant role in various biological processes and is primarily used in the food industry and in the production of certain types of plastics and resins.

Check Digit Verification of cas no

The CAS Registry Mumber 18545-28-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,4 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18545-28:
(7*1)+(6*8)+(5*5)+(4*4)+(3*5)+(2*2)+(1*8)=123
123 % 10 = 3
So 18545-28-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O3/c1-5(7)8-4-2-3-6/h3H,2,4H2,1H3

18545-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Oxopropyl acetate

1.2 Other means of identification

Product number -
Other names 3-acetoxypropanal

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:18545-28-3 SDS

18545-28-3Relevant articles and documents

Asymmetric hydroformylation of vinyl acetate with BINAP-rhodium(I) complexes

Hoegaerts, Dirk,Jacobs, Pierre A.

, p. 3039 - 3043 (1999)

Complexes of (R)-BINAP (BINAP=2,2'-bis(diphenylphosphino)-1,1'-binaphthyl) derived from the available rhodium precursors Rh(acac)(CO)2 and [Rh(μ-OMe)(cod)]2 are used for the asymmetric hydroformylation of vinyl acetate. Enantiomeric excesses of up to 60% are achieved with regioselectivities of up to 99%. Only a BINAP/Rh ratio of 2 is required. Effects of pressure and temperature on catalyst stability, enantio- and chemoselectivity are discussed.

New diphosphite ligands for enantioselective asymmetric hydroformylation

Zou, Yaping,Yan, Yongjun,Zhang, Xumu

, p. 4781 - 4784 (2007)

A series of new diphosphite ligands have been easily prepared from BINOL derivatives; moderate enantioselectivities (up to 80% ee) and excellent regioselectivities (b/l up to 98/2) have been achieved in the Rh-catalyzed asymmetric hydroformylation of vinyl acetate.

Regioselective and rapid hydroformylation of vinyl acetate catalyzed by rhodium complex modified bulky phosphite ligand

Dabbawala, Aasif A.,Jasra, Raksh V.,Bajaj, Hari C.

, p. 616 - 619 (2010)

The regioselective hydroformylation of vinyl acetate catalyzed by rhodium complex of monodentate phosphite ligand, tri-1-naphthylphosphite P(ONp)3, was investigated. The P(ONp)3 ligand exhibited a considerable impact on the rate and selectivity of hydroformylation of vinyl acetate, notably high turnover frequency (up to 11,520 h-1) with excellent regioselectivity (99%) to the preferred branched aldehyde and high selectivity to aldehyde (93%). Significant results with the substrate having less reactive character toward hydroformylation and practically easy accessibility of the ligand (synthesized from inexpensive compound, 1-naphthol) make this system very attractive.

Tetradentate nitrogen phosphine ligand and preparation method and application thereof

-

Paragraph 0057; 0060-0061, (2021/04/07)

The invention provides a novel tetradentate nitrogen phosphine ligand as well as a preparation method and an application thereof in an unsaturated olefin hydroformylation reaction. The tetradentate nitrogen phosphine ligand is used for the hydroformylation reaction of olefin, so that the catalyst is more stable in the reaction, is not easy to inactivate at high temperature (more than 200 DEG C), the pressure of synthesis gas required by the reaction is lower, the reaction positive-to-negative ratio is improved, and the selectivity of a main product can be effectively improved.

Phosphine ligand compound and preparation method thereof, catalyst composition and application thereof and vinyl acetate hydroformylation method (by machine translation)

-

Paragraph 0106-0127, (2020/07/13)

The invention relates to the field of vinyl acetate hydroformylation, and discloses a phosphine ligand compound and a preparation method thereof, a catalyst composition and application of the phosphine ligand compound and vinyl acetate hydroformylation. The phosphine ligand compound has the structure shown in the formula (1); and A and B1 And B2 C is each independently selected from substituted or unsubstituted C1 - C20 Alkylene; and A, B1 And B2 The optionally present substituents are each independently selected from C. 1 - C20 Alkyl, halogen and C1 - C10 The phosphorus ligand compound provided by the invention can effectively improve the vinyl acetate conversion rate and 2 - acetoxy propionaldehyde selectivity. (by machine translation)

Phosphine ligand compound and preparation method thereof, catalyst composition and application thereof and vinyl acetate hydroformylation method (by machine translation)

-

Paragraph 0094-0095; 0106-0107; 0111, (2020/07/13)

The invention relates to the field of vinyl acetate hydroformylation, and discloses a phosphine ligand compound and a preparation method thereof, a catalyst composition and application of the phosphine ligand compound and vinyl acetate hydroformylation. The phosphine ligand compound has the structure shown in the formula (1); wherein A is selected from substituted or unsubstituted phenyl; B1 And B2 C is each independently selected from substituted or unsubstituted C1 - C20 Alkylene; A, B1 And B2 The optionally present substituents are each independently selected from C. 1 - C20 Alkyl, halogen and C1 - C10 The phosphorus ligand compound provided by the invention can effectively improve the vinyl acetate conversion rate and 2 - acetoxy propionaldehyde selectivity. (by machine translation)

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