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Butylidenecyclohexane, also known as 1-methyl-1-cyclohexene, is an organic compound with the molecular formula C10H18. It is a colorless liquid that is insoluble in water but soluble in organic solvents. This cyclic alkene is formed by the addition of a butyl group to the cyclohexane ring, resulting in a structure that contains a double bond between two carbon atoms. Butylidenecyclohexane is used as a chemical intermediate in the synthesis of various organic compounds, such as fragrances, pharmaceuticals, and other specialty chemicals. It is also known for its potential use as a fuel additive or a component in the production of polymers. Due to its chemical reactivity, it is important to handle butylidenecyclohexane with care, as it can undergo further reactions, such as hydrogenation or halogenation, to produce a variety of derivatives.

2272-03-9

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2272-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2272-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2272-03:
(6*2)+(5*2)+(4*7)+(3*2)+(2*0)+(1*3)=59
59 % 10 = 9
So 2272-03-9 is a valid CAS Registry Number.

2272-03-9SDS

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 butylidenecyclohexane

1.2 Other means of identification

Product number -
Other names Cyclohexane,butylidene

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:2272-03-9 SDS

2272-03-9Relevant academic research and scientific papers

Unsaturated hydrocarbons with fruity and floral odors

Anselmi, Cecilia,Centini, Marisanna,Fedeli, Paola,Paoli, Maria Laura,Sega, Alessandro,Scesa, Carla,Pelosi, Paolo

, p. 1285 - 1289 (2007/10/03)

Hydrocarbons usually do not exhibit odors of interest or well-defined character. However, certain cyclic alkenes have been associated with typical and pleasant notes, such as fruity, green, and floral. One of the best known examples is represented by the

Stereoselective Synthesis of Exocyclic Alkenes via Zirconium-Promoted Alkyl-Diene Coupling

Negishi, Ei-ichi,Miller, Steven R.

, p. 6014 - 6016 (2007/10/02)

The reaction of 1-vinyl-1-cycloalkenes with 1 equiv of (RCH2CH2)2ZrCp2, where R is H or alkyl, followed by treatment with electrophiles, e.g., proton donors, I2, and ketones, can provide the corresponding exocyclic alkenes in good yields, the stereoselect

Anwendungen der Phasentransfer-Katalyse 17. Wittig-Reaktionen in verschiedenen Zweiphasen-Systemen

Dehmlow, Eckehard V.,Barahona-Naranjo, Simon

, p. 1748 - 1762 (2007/10/02)

EINE vergleichende Untersuchung von Wittig-Reaktionen unter Phasentransfer-Katalyse (PTC) bei verschiedenen Bedingungen wurde durchgefuehrt.Es erwies sich als unnoetig, ausser den Phosphoniumsalzen einen PTC-Katalysator zu verwenden.Mechanistische Konsequenzen dieses Befundes werden diskutiert.Als ein besonders geeignetes Basensystem stellte sich Kalium-tert-butoxid in Benzol heraus.Erstmals gelang die Umzetzung von Ketonen und aliphatischen Aldehyden.Einige sehr hohe Literaturausbeuten von PTC-Wittig-Reaktionen konnten unter praeparativen Bedingungen nicht reproduziert werden.

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