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2,3-Decadiene, 4-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91948-39-9

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91948-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91948-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,4 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91948-39:
(7*9)+(6*1)+(5*9)+(4*4)+(3*8)+(2*3)+(1*9)=169
169 % 10 = 9
So 91948-39-9 is a valid CAS Registry Number.

91948-39-9SDS

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 4-ethyldeca-2,3-diene

1.2 Other means of identification

Product number -
Other names 2,3-Decadiene,4-ethyl

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:91948-39-9 SDS

91948-39-9Downstream Products

91948-39-9Relevant articles and documents

Allenes and Acetylenes. 28. On the Mechanism of Reduction of Propargylic Ethers and Acetates with Organocuprates

Sahlberg, Christer,Claesson, Alf

, p. 4120 - 4122 (2007/10/02)

The amounts of substitution and reduction products from the reaction of two types of propargylic methyl ethers and acetates with organocuprates were determined.The methyl ethers give rise to more of the reduction products than the acetates.It is shown that "reduced" allenes are formed by hydrolysis of an organometallic intermediate whereas "reduced" acetyles are formed mainly by another mechanistic pathway.The mechanisms of these reduction reactions are discussed in terms of stabilized, transient Cu(III)-intermediates and concerted β-hydride transfer in the formation of the acetylene.

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