Welcome to LookChem.com Sign In|Join Free
  • or
2-Cyclopenten-1-one, 5-methylene-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79655-71-3

Post Buying Request

79655-71-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

79655-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79655-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,5 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79655-71:
(7*7)+(6*9)+(5*6)+(4*5)+(3*5)+(2*7)+(1*1)=183
183 % 10 = 3
So 79655-71-3 is a valid CAS Registry Number.

79655-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylidene-2-phenylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 5-methylene-2-phenylcyclopent-2-en-1-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:79655-71-3 SDS

79655-71-3Relevant academic research and scientific papers

Short synthesis of methylenecyclopentenones by intermolecular Pauson-Khand reaction of allyl thiourea

Petrovski, ?eljko,Martins, Bruno M.R.,Afonso, Carlos A.M.

supporting information; experimental part, p. 3356 - 3359 (2010/08/19)

N,N,N′-Trimethylallylthiourea promotes the intermolecular Pauson-Khand reaction with alkynes in the presence of Co2(CO)8 and moderate pressure of CO followed by thiourea elimination allowing the formation of methylenecyclopentenone d

Rearrangement of allylic and propargylic alcohols catalyzed by the combined use of tetrabutylammonium perrhenate(VII) and p-toluenesulfonic acid

Narasaka,Kusama,Hayashi

, p. 2059 - 2068 (2007/10/02)

Allylic rearrangement and/or dehydration reaction of allylic alcohols proceeds smoothly by the use of catalytic amounts of tetrabutylammonium perrhenate and p-toluenesulfonic acid hydrate. Treatment of propargylic alcohols with the catalysts at room temperature affords the rearranged products, α,β-unsaturated carbonyl compounds, while β,γ-unsaturated ketones are obtained as main products by the reaction in refluxing 1,2-dichloroethane. The application of this catalytic system is also described for the preparation of some synthetic intermediates.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 79655-71-3