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3-Buten-2-one, 4-cyclopropyl-, (E)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105891-18-7

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105891-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105891-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,9 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105891-18:
(8*1)+(7*0)+(6*5)+(5*8)+(4*9)+(3*1)+(2*1)+(1*8)=127
127 % 10 = 7
So 105891-18-7 is a valid CAS Registry Number.

105891-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3E)-4-cyclopropyl-3-butene-2-one

1.2 Other means of identification

Product number -
Other names 4-cyclopropyl-3(E)-buten-2-one

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:105891-18-7 SDS

105891-18-7Downstream Products

105891-18-7Relevant academic research and scientific papers

Selectivity in nickel-catalyzed rearrangements of cyclopropylen-ynes

Zuo, Gang,Louie, Janis

, p. 5798 - 5799 (2005)

The Ni/NHC-catalyzed rearrangement of cyclopropylen-ynes is described. Two different heterocycles, cyclopentane- or cycloheptene-based, were obtained. However, by employing ItBu as the NHC ligand, cyclopentane products were obtained selectively under mild

Reprint of: Synthesis of a tricyclic core of rameswaralide

Trost, Barry M.,Nguyen, Hien M.,Koradin, Christopher

, p. 2033 - 2036 (2011)

A tricyclic core containing a 5,7-fused bicyclic unit of rameswaralide was prepared starting from a 1,6-enyne. The synthetic sequence involved (i) ruthenium-catalyzed [5+2]-cycloaddition of 1,6-enyne, (ii) an acyl radical based approach to construct the lactone, and (iii) a regioselective installation of the conjugated double bond by a concomitant sulfenylation - dehydrosulfenylation sequence. 2010 Elsevier Ltd. All rights reserved.

Synthesis of a tricyclic core of rameswaralide

Trost, Barry M.,Nguyen, Hien M.,Koradin, Christopher

supporting information; experimental part, p. 6232 - 6235 (2011/01/12)

A tricyclic core containing a 5,7-fused bicyclic unit of rameswaralide was prepared starting from a 1,6-enyne. The synthetic sequence involved (i) ruthenium-catalyzed [5+2]-cycloaddition of 1,6-enyne, (ii) an acyl radical based approach to construct the lactone, and (iii) a regioselective installation of the conjugated double bond by a concomitant sulfenylation-dehydrosulfenylation sequence.

STRUCTURE OF ACETYL FLUOROSULFATE. ACYLATION OF CYCLOPROPYL-SUBSTITUTED ALKENES WITH ACETYL FLUOROSULFATE

Gavrishova, T. N.,Shastin, A. V.,Balenkova, E. S.

, p. 402 - 406 (2007/10/02)

By methods of IR and 1H, 13C, and 19F NMR spectroscopy it was shown that acetyl fluorosulfate formed in the reaction of acetyl fluoride with SO3 exists in the covalent form.The acylation of cyclopropane-substituted alkenes (vinyl- and isopropenyl-cyclopropanes, 1,1-dicyclopropylethylene, 1-methyl-1-vinyl- and 1-isopropenyl-1-methyl-cyclopropanes) with acetyl fluorosulfate goes without the rearrangement of the carbon skeleton, and it enables us to prepare functional derivatives of cyclopropane in preparative yields.

Chemistry and structure-activity relationships of C-17 unsaturated 18-cycloalkyl and cycloalkyl analogues of enisoprost. Identification of a promising new antiulcer prostaglandin

Collins,Gasiecki,Perkins,Gullikson,Bianchi,Kramer,Ng,Yonan,Swenton,Jones,Bauer

, p. 2784 - 2793 (2007/10/02)

A series of Δ17 unsaturated cycloalkyl and cycloalkenyl analogues of enisoprost was synthetized to investigate the effects of ω chain unsaturation on gastric antisecretory activity and diarrheogenic side effects. Of these, the 17E, 18-cyclopent

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