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Cyclopentanone, 2-(1-methylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58070-36-3

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58070-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58070-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,7 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58070-36:
(7*5)+(6*8)+(5*0)+(4*7)+(3*0)+(2*3)+(1*6)=123
123 % 10 = 3
So 58070-36-3 is a valid CAS Registry Number.

58070-36-3SDS

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 2-prop-1-en-2-ylcyclopentan-1-one

1.2 Other means of identification

Product number -
Other names 2-isopropenylcyclopentanone

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:58070-36-3 SDS

58070-36-3Downstream Products

58070-36-3Relevant academic research and scientific papers

Origin of the Regiochemistry in the Photochemical Cycloaddition Reaction of 2-Cyclopentenone with Allene: Trapping of Triplet 1,4-Biradical Intermediates with Hydrogen Selenide

Maradyn, David J.,Sydnes, Leiv K.,Weedon, Alan C.

, p. 2413 - 2416 (2007/10/02)

The photochemical cycloaddition reaction between 2-cyclopentenone and allene in toluene at -78 deg C yields cyclobutane adducts with head-to-head and head-to-tail regiochemistry in a ratio of 88:12.In the presence of high concentrations of hydrogen seleni

PHOTOCLEAVAGE OF CARBON-TIN BOND ACTIVATED BY NEIGHBORING

Sato, Tadashi,Takezoe, Kohji

, p. 4003 - 4006 (2007/10/02)

β-Stannyl ketones underwent various types of reaction upon UV-irradiation, depending upon the substitution pattern of the substrate, and upon the solvent used.

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