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1,3-Cycloundecadiene is a cyclic alkene with the molecular formula C11H18. It is a colorless liquid with a strong, pungent odor. This organic compound consists of a cycloalkane ring with eleven carbon atoms, featuring two carbon-carbon double bonds at positions 1 and 3. It is an important intermediate in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and fragrances. Due to its reactive nature, 1,3-cycloundecadiene is often used in Diels-Alder reactions, a type of cycloaddition reaction that forms six-membered rings. The compound is also known for its potential applications in polymer chemistry and as a precursor to other valuable organic compounds.

6568-16-7

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6568-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6568-16-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6568-16:
(6*6)+(5*5)+(4*6)+(3*8)+(2*1)+(1*6)=117
117 % 10 = 7
So 6568-16-7 is a valid CAS Registry Number.

6568-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name cycloundeca-1,3-diene

1.2 Other means of identification

Product number -
Other names 1,3-Cycloundecadiene

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:6568-16-7 SDS

6568-16-7Downstream Products

6568-16-7Relevant academic research and scientific papers

Preparation and Pyrolysis of Stereoisomeric Bromobicycloalkanes (n = 6, 8, 10)

Dehmlow, Eckehard V.,Kramer, Roland

, p. 489 - 494 (2007/10/02)

The title compounds 1a-3c were prepared by stereoselective reduction of the respective dibromides.Pyrolysis gave allylic bromides (8, 9, 11) as primary and dienes (10, 12) as secondary products.Product ratios were independent of the stereochemistry of the starting materials.No differences of the rearrangement rates of the stereoisomers were observed in gas phase reactions of the derivatives of bicyclo- and bicycloalkanes.With the larger bicyclo derivatives, however, distinct differences in the thermal stability of cis-/trans-isomers 4c/5c or 2c/3c were found in condensed phase. - Keywords: Dibromocarbene Adducts, Stereoselective Debromination, Rearrangement, Allylic Bromides

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