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4974-27-0

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4974-27-0 Usage

Definition

ChEBI: An alkadiene that is octane with the two double bonds located at positions 2 and 6.

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 2654, 1951 DOI: 10.1021/ja01150a068

Check Digit Verification of cas no

The CAS Registry Mumber 4974-27-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,7 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4974-27:
(6*4)+(5*9)+(4*7)+(3*4)+(2*2)+(1*7)=120
120 % 10 = 0
So 4974-27-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-3-5-7-8-6-4-2/h3-6H,7-8H2,1-2H3/b5-3+,6-4+

4974-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-OCTADIENE

1.2 Other means of identification

Product number -
Other names 2,6-Octadiene

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:4974-27-0 SDS

4974-27-0Downstream Products

4974-27-0Relevant articles and documents

REACTIONS INVOLVING TRANSITION METALS. XVII. REACTION OF ORGANIC HALOGEN COMPOUNDS WITH 2 AND 2 (S = CH2Cl2, THF)

Booth, Brian L.,Casey, Geoffrey C.,Haszeldine, Robert N.

, p. 197 - 205 (2007/10/02)

The complexes 2 and 2 (S=CH2Cl2, THF) have been shown to react with CXCl3 (X=Cl, H) to form with generation of both dichlorocarbene and trichloromethyl radical.Reaction of 2 with CF3I, allyl- and benzyl-halides takes a different course giving organic coupling products and .The THF solvate complex also causes coupling of gem-dihalides, and dehalogenation of vic-dihalides to produce alkenes.Possible mechanisms for these reactions are discussed.

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