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19780-56-4

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19780-56-4 Usage

Type of compound

Cyclopentene derivative

Substituents

Ethyl and methyl groups attached to the cyclopentene ring

Usage

+ Production of organic chemicals and polymers
+ Building block for the synthesis of other compounds
+ Precursor in the synthesis of pharmaceuticals and agrochemicals
+ Intermediate in the production of flavors and fragrances
+ Manufacturing of plastics and rubber products

Unique attributes

Unique chemical structure and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 19780-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19780-56:
(7*1)+(6*9)+(5*7)+(4*8)+(3*0)+(2*5)+(1*6)=144
144 % 10 = 4
So 19780-56-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-3-8-6-4-5-7(8)2/h3-6H2,1-2H3

19780-56-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ETHYL-2-METHYLCYCLOPENTENE

1.2 Other means of identification

Product number -
Other names 1-Ethyl-2-methyl-cyclopenten

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:19780-56-4 SDS

19780-56-4Relevant articles and documents

Protium-deuterium exchange of cyclic and acyclic alkanens in dilute acid medium at elevated temperatures

Werstiuk, Nick Henry,Timmins, George

, p. 530 - 533 (2007/10/02)

A modification of the high temperature - dilute acid (HTDA) method for deuterium labelling of aromatic compounds has been applied to the H-D exchange of a number of cyclic and acyclic alkenes.Cyclopentene, cyclohexene, cyclododecene, and tetramethylethylene have been completely exchanged in excellent yield. 1-Methylcyclopentene and 1-methylcyclohexene have also been perdeuterated and cycloheptene and cyclooctene partially labelled but require spinning band distillation or preparative glpc for separation from rearrangement products.A variety of C5-C8 acyclic alkeneshave also been treated under HTDA conditions.

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