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3-Isopropylidene-6-methyl-5-hepten-2-one is a complex organic compound with the molecular formula C11H18O. It is a colorless liquid with a strong, pungent odor. 3-Isopropylidene-6-methyl-5-hepten-2-one is characterized by the presence of an isopropyl group (C3H7), a methyl group (CH3), and a carbonyl group (C=O). The structure features a conjugated diene system, which is a sequence of two carbon-carbon double bonds separated by a single bond. This specific arrangement of functional groups and the conjugated diene system contribute to its chemical reactivity and potential applications in the synthesis of various organic compounds. It is commonly used in the fragrance industry and as a chemical intermediate in the production of other chemicals.

2520-63-0

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2520-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2520-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2520-63:
(6*2)+(5*5)+(4*2)+(3*0)+(2*6)+(1*3)=60
60 % 10 = 0
So 2520-63-0 is a valid CAS Registry Number.

2520-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-3-propan-2-ylidenehept-5-en-2-one

1.2 Other means of identification

Product number -
Other names prenyl mesityl oxide

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:2520-63-0 SDS

2520-63-0Downstream Products

2520-63-0Relevant academic research and scientific papers

Process for the production of unsaturated ketones

-

, (2008/06/13)

There is disclosed a process for preparing unsaturated ketones especially terpenoid ketones, by subjecting a substituted propargyl alcohol of formula (II) STR1 wherein R is a group containing 1 or 2 substituted or unsubstituted alkyl- or alkylene units containing 4 carbon atoms each to a thermal treatment sufficient to rearrange its structure in order to obtain structurally isomeric unsaturated ketones of formula I STR2 wherein one of the substituents X3 and X4 is hydrogen and the other and Z2 together form a bond. The process can be effected in the presence of an isomerization catalyst, which leads to high percentage of α.β,γ.δ-unsaturated ketones. The ketones of formula I are useful as perfumes and as intermediates for the production of terpenoid compounds.

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