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Cyclohexene, 4,5-dimethyl- is an organic compound with the chemical formula C8H14. It is a cyclic hydrocarbon with a six-carbon ring structure, where two methyl groups are attached to the 4th and 5th carbon atoms. Cyclohexene, 4,5-dimethyl- is a colorless liquid with a pungent odor and is insoluble in water. It is used as a chemical intermediate in the synthesis of various organic compounds, such as pharmaceuticals, agrochemicals, and fragrances. Due to its reactive nature, it is important to handle Cyclohexene, 4,5-dimethyl- with care, as it can be flammable and may cause irritation to the skin, eyes, and respiratory system.

4300-00-9

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4300-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4300-00-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,0 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4300-00:
(6*4)+(5*3)+(4*0)+(3*0)+(2*0)+(1*0)=39
39 % 10 = 9
So 4300-00-9 is a valid CAS Registry Number.

4300-00-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dimethylcyclohexene

1.2 Other means of identification

Product number -
Other names Cyclohexene,4,5-dimethyl

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:4300-00-9 SDS

4300-00-9Relevant academic research and scientific papers

METHODS OF PREPARING PARA-XYLENE FROM BIOMASS

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Page/Page column 23, (2013/11/05)

Methods or preparing para-xylene from biomass by carrying out a Diels-Alder cycloaddition at controlled temperatures and activity ratios. Methods of preparing bio- terephthalic acid and bio-poly(ethylene terephthalate (bio-PET) are also disclosed, as well as products formed from bio-PET.

A Total Synthesis of (+/-)-Faranal, the True Trail Pheromone of Pharaoh's Ant, Monomorium pharaonis

Knight, David W.,Ojhara, Bol

, p. 955 - 960 (2007/10/02)

A relatively short total synthesis of the true trail pheromone of Pharaoh's ant, (+/-)-faranal is reported.The carbon skeleton was assembled by a Wittig condensation between (Z)-6-methyloct-5-en-2-one (4) and the 5-carboxypentylphosphonium salt (15).The ketone (4) was prepared in 'one-pot' and in a stereoselective manner using vinyl cuprate chemistry, while the relative stereochemistry of the two methyl substituents in the phosphonium salt (15) was established by using the Diels-Alder adduct (16) of buta-1,3-diene and maleic anhydride, which, after reduction and oxidative cleavage of the resulting cis-1,2-dimethylcyclohex-4-ene (18), gave only meso-3,4-dimethyladipic acid (19); this in turn was converted into the salt (15) in six straight-forward steps.

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