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dicyclopent-1-en-1-ylmethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58866-22-1

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58866-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58866-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,6 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58866-22:
(7*5)+(6*8)+(5*8)+(4*6)+(3*6)+(2*2)+(1*2)=171
171 % 10 = 1
So 58866-22-1 is a valid CAS Registry Number.

58866-22-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name di(cyclopenten-1-yl)methanone

1.2 Other means of identification

Product number -
Other names dicyclopent-1-enyl 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:58866-22-1 SDS

58866-22-1Relevant academic research and scientific papers

The reductive Nazarov cyclization

Giese, Soeren,West

, p. 8393 - 8396 (2007/10/03)

Tri- and tetrasubstituted 1,4-dien-3-ones 1 were treated with Lewis acid in the presence of triethylsilane, furnishing either silyl enol ethers 4 or cyclopentanones 5 in good yields, depending upon work-up conditions. This reaction is presumed to occur th

A NEW APPROACH TO CYCLOPENTANE ANNULATED COMPOUNDS VIA 1-(CYCLOPENT-1-ENYLCARBONYL)VINYLPHOSPHONATES, AND SYNTHESIS AND SYNTHETIC APPLICATION OF α-DIETHOXYPHOSPHORYL-Δα,β-BUTENOLIDES

Minami, Toru,Nakayama, Minoru,Fujimoto, Kouichi,Matsuo, Shingo

, p. 135 - 138 (2007/10/02)

Fused ring systems, containing two or three five-membered rings, were constructed by utilizing 1-(cyclopent-1-enylcarbonyl)vinylphosphonates which function as versatile annulating agents.Facile synthesis of α,β-carbocyclic fused γ-lactones was provided by

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