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19639-00-0

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19639-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19639-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,3 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19639-00:
(7*1)+(6*9)+(5*6)+(4*3)+(3*9)+(2*0)+(1*0)=130
130 % 10 = 0
So 19639-00-0 is a valid CAS Registry Number.

19639-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-5-methyloxolan-2-one

1.2 Other means of identification

Product number -
Other names dihydro-3-ethyl-5-methyl-2(3H)-furanone

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:19639-00-0 SDS

19639-00-0Downstream Products

19639-00-0Relevant articles and documents

A convenient method for lactonization of α-allyl esters using iodine in dimethylsulphoxide

Nawghare, Beena R.,Gaikwad, Sunil V.,Pawar, Bharati V.,Lokhande, Pradeep D.

, p. 469 - 473 (2014/12/11)

A simple method for the synthesis of α-γ-disubstituted-γ-butyrolactones by cyclization of α-allyl esters using iodine in dimethylsulphoxide is reported. This method is efficient and operationally simple in comparison to methods using transition metal comp

SIMPLE SYNTHESIS OF γ-LACTONES FROM OLEFINIC NITRILES

Tiecco, Marcello,Tingoli, Marco,Testaferri, Lorenzo,Bartoli, Donatella

, p. 2817 - 2824 (2007/10/02)

The reaction of substituted 4-pentenonitriles with 50 percent sulphuric acid at 100 deg C afforded γ-lactones in moderate to good yield.

A Novel Route to α-Substituted γ-Lactones via Lactone Enolates

Jedlinski, Zbigniew,Kowalczuk, Marek,Kurcok, Piotr,Grzegorzek, Miroslaw,Ermel, Jolanta

, p. 4601 - 4602 (2007/10/02)

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