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(3E)-Hepta-1,3-diene is an organic compound with the molecular formula C7H12. It is a conjugated diene, which means it has two carbon-carbon double bonds separated by a single bond, in this case, located at the 1st and 3rd carbon atoms. The "E" configuration indicates that the double bonds have a trans (E) orientation, with the substituents on the double bonds being on opposite sides of the molecule. (3E)-hepta-1,3-diene is a colorless liquid with a strong, pungent odor and is used as a building block in the synthesis of various organic compounds, including pharmaceuticals and polymers. It is also known for its reactivity in Diels-Alder reactions, a type of chemical reaction that involves the cycloaddition of a conjugated diene with an alkene or alkyne.

2384-92-1

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2384-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2384-92-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2384-92:
(6*2)+(5*3)+(4*8)+(3*4)+(2*9)+(1*2)=91
91 % 10 = 1
So 2384-92-1 is a valid CAS Registry Number.

2384-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3E)-hepta-1,3-diene

1.2 Other means of identification

Product number -
Other names trans-Hepta-1,3-dien

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 -
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More Details:2384-92-1 SDS

2384-92-1Relevant academic research and scientific papers

A SIMPLE SYNTHESIS OF 1-TRIMETHYLSILYL-2,3-DIENES

Nativi, Cristina,Ricci, Alfredo,Taddei, Maurizio

, p. 2751 - 2752 (2007/10/02)

1-Trimethylsilyl-2,3-dienes have been prepared through a conjugative acidic elimination of a tributylstannyl and a hydroxy group from β-hydroxy-vinylstannanes.

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