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2-Methyl-5-isopropylcyclopentanone is a cyclic ketone with the molecular formula C9H16O. It features a cyclopentanone ring structure, with a methyl group (CH3) at the 2-position and an isopropyl group (C3H7) at the 5-position. This organic compound is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and fragrances. Due to its complex structure, it is often synthesized through multi-step processes, involving reactions like aldol condensation and dehydration. The compound's stability, reactivity, and potential uses make it an interesting subject for research in organic chemistry.

6784-18-5

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6784-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6784-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6784-18:
(6*6)+(5*7)+(4*8)+(3*4)+(2*1)+(1*8)=125
125 % 10 = 5
So 6784-18-5 is a valid CAS Registry Number.

6784-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-isopropyl-5-methylcyclopentanone

1.2 Other means of identification

Product number -
Other names 2-isopropyl-5-methyl-cyclopentanone

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

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More Details:6784-18-5 SDS

6784-18-5Relevant academic research and scientific papers

Free-radical-mediated Carbonylative Cyclization of Alk-4-enyl Halides Leading to Cyclopentanone

Ryu, Ilhyong,Kusano, Kazuya,Hasegawa, Mitsuharu,Kambe, Nobuaki,Sonoda, Noboru

, p. 1018 - 1019 (2007/10/02)

Alk-4-enyl bromides and iodides 1, when treated with the tributyltin hydride/CO sustem, undergo carbonylative cyclization to give cyclopentanones in good yields (AIBN cat., benzene, 79-90 atm, = 0.025-0.05 mol dm-3, 80 deg C.

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