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2-Cyclopenten-1-one, 3-butyl-2-methyl- is an organic compound with the molecular formula C9H14O. It is a derivative of cyclopentenone, featuring a five-membered ring with a ketone group at position 1, a methyl group at position 2, and a butyl group at position 3. 2-Cyclopenten-1-one, 3-butyl-2-methyl- is characterized by its unique structure, which contributes to its chemical properties and potential applications. It is primarily used in the synthesis of various organic compounds and as an intermediate in the production of pharmaceuticals and other specialty chemicals. Due to its reactive ketone and cyclopentenone functionalities, it can participate in a range of chemical reactions, such as nucleophilic addition, oxidation, and reduction, making it a versatile building block in organic synthesis.

5760-60-1

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5760-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5760-60-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,6 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5760-60:
(6*5)+(5*7)+(4*6)+(3*0)+(2*6)+(1*0)=101
101 % 10 = 1
So 5760-60-1 is a valid CAS Registry Number.

5760-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butyl-2-methylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-methyl-3-butyl-2-cyclopentenone

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:5760-60-1 SDS

5760-60-1Upstream product

5760-60-1Downstream Products

5760-60-1Relevant academic research and scientific papers

Reaction of cyclic α-hydroxy epoxides with a strong base: A new 1,2-rearrangement, evidence for a carbenoid pathway

Doris, Eric,Dechoux, Luc,Mioskowski, Charles

, p. 12700 - 12704 (1995)

Several substituted five- and six-membered cyclic α,β-unsaturated ketones are readily available by treatment of the corresponding α-hydroxy epoxides with an organolithium reagent. The reaction involves a new carbenoid 1,2-alkyl rearrangement. Evidence for the carbenoid intermediate has been obtained by an intramolecular trapping of the highly reactive species.

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