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1,3-Cyclohexadiene, 5-ethyl-1,5-dimethyl- is an organic compound with the molecular formula C10H16. It is a cyclic hydrocarbon with a six-membered ring structure, containing two double bonds between carbon atoms 1 and 3. The molecule has an ethyl group attached to the 5th carbon and two methyl groups attached to the 1st and 5th carbons, respectively. 1,3-Cyclohexadiene, 5-ethyl-1,5-dimethyl- is a derivative of cyclohexadiene and is characterized by its unique structure and properties. It is used in various chemical reactions and synthesis processes, particularly in the production of polymers and other organic compounds. Due to its complex structure, it is essential to handle 1,3-Cyclohexadiene, 5-ethyl-1,5-dimethyl- with care and follow proper safety guidelines during its use and storage.

6521-10-4

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6521-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6521-10-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,2 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6521-10:
(6*6)+(5*5)+(4*2)+(3*1)+(2*1)+(1*0)=74
74 % 10 = 4
So 6521-10-4 is a valid CAS Registry Number.

6521-10-4SDS

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 5-ethyl-1,5-dimethyl-cyclohexa-1,3-diene

1.2 Other means of identification

Product number -
Other names 1,5-Dimethyl-5-aethylcyclohexa-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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6521-10-4 SDS

6521-10-4Relevant academic research and scientific papers

The Pyrolysis of Limonene: a Reappraisal

Traynor, Sean G.,Crowley, Kevin J.,Cocker, Wesley

, p. 2101 - 2115 (2007/10/02)

The pyrolysis of limonene has been re-examined.It involves a high activation energy process in which a biradical is produced initially.This biradical can reform limonene, give a new optically active product, 1,5-dimethyl-5-vinylcyclohexene, or undergo a series of rearrangements to yield a pyrolysis mixture similar to that obtained on pyrolysis of α-pinene.

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