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24253-30-3

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24253-30-3 Usage

Synthesis Reference(s)

Synthesis, p. 1025, 1982 DOI: 10.1055/s-1982-30049

Check Digit Verification of cas no

The CAS Registry Mumber 24253-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,5 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24253-30:
(7*2)+(6*4)+(5*2)+(4*5)+(3*3)+(2*3)+(1*0)=83
83 % 10 = 3
So 24253-30-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O/c1-3-5-6(7)4-2/h3H,1,4-5H2,2H3

24253-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name hex-5-en-3-one

1.2 Other means of identification

Product number -
Other names Aethyl-allyl-keton

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:24253-30-3 SDS

24253-30-3Relevant articles and documents

Mn(III)-salan/graphene oxide/magnetite nanocomposite as a highly selective catalyst for aerobic epoxidation of olefins

Abbasi, Vahideh,Hosseini-Monfared, Hassan,Hosseini, Seyed Majid

, (2017/02/05)

A nanocomposite was synthesized using carbon-coated Fe3O4 nanoparticle-decorated reduced graphene oxide as a convenient and efficient supporting material for grafting of a manganese–reduced Schiff base (salan) complex via covalent attachment. The nanocomposite was characterized using X-ray diffraction, Fourier transform infrared and diffuse reflectance UV–visible spectroscopies, inductively coupled plasma atomic emission spectrometry and scanning electron microscopy. It was evaluated as a catalyst for the aerobic epoxidation of olefins in acetonitrile in combination with a sacrificial co-reductant (isobutyraldehyde). The catalytic performance of the heterogeneous system of the Mn–salan complex is superior to that of the homogeneous one. The catalyst activity strongly depends on the reaction temperature and nature of the solvent. The epoxide yield increases with the nucleophilic character of the olefin. The nanocomposite performs well as an epoxidation catalyst for electron-rich and conjugated olefins. It can be recovered from the reaction medium by magnetic decantation and reused, maintaining good catalytic activity. Copyright

IMPROVED SYNTHESIS OF β,γ-UNSATURATED KETONES BY THE REACTION OF ALLYLIC ZINC BROMIDES WITH NITRILES.

Rousseau, G.,Conia, J. M.

, p. 649 - 652 (2007/10/02)

The reaction of allylic bromides with nitriles in the presence of Zn-Ag couple leads, after hydrolysis, to β,γ-unsaturated ketones in high yield.

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