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2,6-DIMETHYL-3-HEPTENE, also known as alloocimene, is a colorless liquid compound with a strong, fruity odor. It is a naturally occurring chemical found in various plants and fruits, including citrus fruits, mint, and basil. This chemical is commonly used in the fragrance and flavor industry due to its pleasant aroma. It is also employed as a starting material in the synthesis of other organic compounds. In addition, 2,6-DIMETHYL-3-HEPTENE has been studied for its potential biological activities, including antimicrobial and insecticidal properties. Overall, this chemical compound has a wide range of applications in various industries, making it a valuable and versatile substance.

2738-18-3

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2738-18-3 Usage

Uses

Used in Fragrance and Flavor Industry:
2,6-DIMETHYL-3-HEPTENE is used as a fragrance and flavoring agent for its strong, fruity odor and pleasant aroma.
Used in Chemical Synthesis:
2,6-DIMETHYL-3-HEPTENE is used as a starting material for the synthesis of other organic compounds.
Used in Antimicrobial Applications:
2,6-DIMETHYL-3-HEPTENE is used as an antimicrobial agent for its potential biological activity against certain microorganisms.
Used in Insecticidal Applications:
2,6-DIMETHYL-3-HEPTENE is used as an insecticide for its potential biological activity against certain insects.

Check Digit Verification of cas no

The CAS Registry Mumber 2738-18-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2738-18:
(6*2)+(5*7)+(4*3)+(3*8)+(2*1)+(1*8)=93
93 % 10 = 3
So 2738-18-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H18/c1-8(2)6-5-7-9(3)4/h5-6,8-9H,7H2,1-4H3/b6-5+

2738-18-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethylhept-3-ene

1.2 Other means of identification

Product number -
Other names 2,6-dimethyl-hept-3-ene

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:2738-18-3 SDS

2738-18-3Downstream Products

2738-18-3Relevant academic research and scientific papers

Synthesis of Acetone-Derived C6, C9, and C12Carbon Scaffolds for Chemical and Fuel Applications

Moore, Cameron M.,Jenkins, Rhodri W.,Janicke, Michael T.,Kubic, William L.,Polikarpov, Evgueni,Semelsberger, Troy A.,Sutton, Andrew D.

, p. 3382 - 3386 (2016/12/27)

A simple, inexpensive catalyst system (Amberlyst 15 and Ni/SiO2–Al2O3) is described for the upgrading of acetone to a range of chemicals and potential fuels. Stepwise hydrodeoxygenation of the produced ketones can yield branched alcohols, alkenes, and alkanes. An analysis of these products is provided, which demonstrates that this approach can provide a product profile of valuable bioproducts and potential biofuels.

A convenient synthesis of episulfides and their conversion into alkenes

Dybowski, Piotr,Skowrońska, Aleksandra

, p. 1134 - 1136 (2007/10/03)

A convenient and stereoselective synthesis of episulfides based on the reaction of readily available S-(β-oxoalkyl) thiophosphate with sodium borohydride and their conversion into alkenes is described.

Synthesis of Olefins from α-Chlorocarbonyl Compounds

Barluenga, Jose,Yus, Miguel,Concellon, Jose M.,Bernad, Pablo

, p. 677 - 692 (2007/10/02)

Olefins or diolefins with the double bonds in predetermined positions are obtained in moderate to good yields by treatment of α-chlorocarbonyl compounds with Grignard reagents and lithium in a single process.

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