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3-(3-Methyl-2-butenyl)-6-methyl-5-hepten-2-one is a complex organic compound with the molecular formula C12H20O. It is a colorless to pale yellow liquid with a strong, pungent odor. This molecule is characterized by a 5-hepten-2-one backbone, which includes a 3-methyl-2-butenyl group attached to the 3rd carbon and a 6-methyl group on the 6th carbon. It is an important component in the synthesis of various fragrances and flavors, particularly those with citrus or fruity notes. The compound is also known for its potential applications in the pharmaceutical industry. Due to its reactive nature, it is typically handled with care in a controlled environment to prevent unwanted reactions or decomposition.

2753-03-9

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2753-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2753-03-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2753-03:
(6*2)+(5*7)+(4*5)+(3*3)+(2*0)+(1*3)=79
79 % 10 = 9
So 2753-03-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H22O/c1-10(2)6-8-13(12(5)14)9-7-11(3)4/h6-7,13H,8-9H2,1-5H3

2753-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-3-(3-methylbut-2-enyl)hept-5-en-2-one

1.2 Other means of identification

Product number -
Other names 2.8-Dimethyl-5-acetyl-nonadien-(2.7)

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 -
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More Details:2753-03-9 SDS

2753-03-9Relevant academic research and scientific papers

Stereo- and regioselectivity of intramolecular 1,2-arene-alkene photocycloaddition in 2-alkenyl-4-chromanones

Kalena, Govind P.,Pradhan, Padmanava,Banerji, Asoke

, p. 3209 - 3218 (2007/10/03)

Intramolecular 1,2-arene-alkene photocycloaddition of 2-alkenyl-4- chromanones gave complex multicyclic oxatetracyclotetradecanediones which on internal photo- and microwave induced thermal rearrangements provided a diverse array of compounds with [3.3.0]bicyclooctane carbon frame work. The stereo-and regiochemical aspects as well as desymmetrization of alkenyl chromanones due to intramolecular 1,2-arene-alkene photocycloaddition have also been discussed.

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