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2-Selenabicyclo[2.2.2]oct-5-ene-3,3-dicarboxylic acid, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139059-79-3

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139059-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139059-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,5 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 139059-79:
(8*1)+(7*3)+(6*9)+(5*0)+(4*5)+(3*9)+(2*7)+(1*9)=153
153 % 10 = 3
So 139059-79-3 is a valid CAS Registry Number.

139059-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 3-selenabicyclo[2.2.2]oct-5-ene-2,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2-Selenabicyclo[2.2.2]oct-5-ene-3,3-dicarboxylic acid,diethyl ester

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:139059-79-3 SDS

139059-79-3Downstream Products

139059-79-3Relevant academic research and scientific papers

Preparation and Cycloaddition Chemistry of Thio- and Selenocarbonyls Derived from Reaction of Elemental Sulfur and Selenium with Stabilized α-Halo Anions

Abelman, Matthew M.

, p. 7389 - 7392 (2007/10/02)

Reaction of diethyl chloromalonate with Cs2CO3 in the presence of elemental S8 or Sen generates the corresponding diethyl thioxo- or selenoxomalonates which are subsequently trapped in situ with various 1,3-dienes.Similarly, the chalcogen carbonyls can be prepared from other halogenated compounds using DBU as the base and effectively trapped in Diels-Alder fashion with 2,3-dimethyl-1,3-butadiene (Table 2).

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