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2918-13-0

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2918-13-0 Usage

Definition

ChEBI: An enone that is hept-1-ene substituted by an oxo group at position 3.

Synthesis Reference(s)

Canadian Journal of Chemistry, 52, p. 3825, 1974 DOI: 10.1139/v74-572

Check Digit Verification of cas no

The CAS Registry Mumber 2918-13-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2918-13:
(6*2)+(5*9)+(4*1)+(3*8)+(2*1)+(1*3)=90
90 % 10 = 0
So 2918-13-0 is a valid CAS Registry Number.

2918-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hepten-3-one

1.2 Other means of identification

Product number -
Other names Vinyl butyl ketone

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:2918-13-0 SDS

2918-13-0Relevant articles and documents

Selective oxidation of styrene catalyzed by cerium-doped cobalt ferrite nanocrystals with greatly enhanced catalytic performance

Tong, Jinhui,Li, Wenyan,Bo, Lili,Wang, Huan,Hu, Yusen,Zhang, Zhixia,Mahboob, Abdulla

, p. 474 - 481 (2016/11/18)

The rare earth metal Ce-doped cobalt ferrite samples CexCo1?xFe2O4 (x?=?0.1, 0.3, 0.5) were prepared by the sol–gel autocombustion route. The as-prepared samples were characterized by X-ray diffractometry, scanning electron microscopy, transmission electron microscopy, ICP–atomic emission spectroscopy, and N2 physisorption. Their catalytic performance was evaluated in oxidation of styrene using hydrogen peroxide (30%) as oxidant. Compared with pristine CoFe2O4, the Ce-doped samples were found to be more efficient catalysts for the oxidation of styrene to benzaldehyde, with greatly enhanced catalytic performance. Especially, when Ce0.3Co0.7Fe2O4 was used as catalyst, 90.3% styrene conversion and 91.5% selectivity for benzaldehyde were obtained at 90?°C for 9?h reaction. The catalyst can be magnetically separated easily for reuse, and no obvious loss of activity was observed when it was reused in five consecutive runs.

Solid Lewis acids catalyze the carbon-carbon coupling between carbohydrates and formaldehyde

Van De Vyver, Stijn,Odermatt, Caroline,Romero, Kevin,Prasomsri, Teerawit,Román-Leshkov, Yuriy

, p. 972 - 977 (2015/09/08)

The development of catalytic C-C bond formation schemes based on renewable substrates is important for defining sustainable paradigms for chemical manufacturing. With a few exceptions, aldol condensation reactions between biomass-derived platform chemicals have received little attention so far. Here the C-C coupling between 1,3-dihydroxyacetone (DHA) and formaldehyde into α-hydroxy-γ-butyrolactone (HBL) using Sn-Beta is demonstrated. Reactivity studies, coupled with spectroscopic and computational analyses, show that the formation of HBL proceeds by soft enolization of DHA followed by an aldol addition of formaldehyde to the Sn-enolate intermediate, generating erythrulose as an intermediate species. Isotopic labeling is used to reveal the position where formaldehyde is incorporated into HBL, providing further support for our proposed mechanism. Finally, combining the C-C coupling reaction with transfer hydrogenation of formaldehyde has allowed us to expand the substrate scope to include polyols glycerol and ethylene glycol.

Preparation of α-methylene ketones by direct methylene transfer

Rodrigues, J. Augusto R.,Siqueira-Filho, Ezequias P.,De Mancilha, Moacir,Moran, Paulo J. S.

, p. 331 - 340 (2007/10/03)

Four methods for the preparation of α-methylene ketones by direct methylene transfer are presented. The procedures were optimized in order to obtain high yields.

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