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19398-85-7

19398-85-7

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19398-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19398-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,9 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19398-85:
(7*1)+(6*9)+(5*3)+(4*9)+(3*8)+(2*8)+(1*5)=157
157 % 10 = 7
So 19398-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-6H,7-10H2,1-2H3/b5-3+,6-4+

19398-85-7SDS

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 trans,trans-2,8-decadiene

1.2 Other means of identification

Product number -
Other names deca-2t,8t-diene

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:19398-85-7 SDS

19398-85-7Downstream Products

19398-85-7Relevant articles and documents

Olefins from biomass feedstocks: Catalytic ester decarbonylation and tandem Heck-type coupling

John, Alex,Hogan, Levi T.,Hillmyer, Marc A.,Tolman, William B.

supporting information, p. 2731 - 2733 (2015/03/05)

With the goal of avoiding the need for anhydride additives, the catalytic decarbonylation of p-nitrophenylesters of aliphatic carboxylic acids to their corresponding olefins, including commodity monomers like styrene and acrylates, has been developed. The reaction is catalyzed by palladium complexes in the absence of added ligands and is promoted by alkali/alkaline-earth metal halides. Combination of catalytic decarbonylation and Heck-type coupling with aryl esters in a single pot process demonstrates the viability of employing a carboxylic acid as a "masked olefin" in synthetic processes. This journal is

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