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2-Methyl-6-methylene-1,7-octadiene is a conjugated diene with the molecular formula C9H14. It is an organic compound characterized by a carbon-carbon double bond at the 2nd and 6th positions, with a methyl group attached to the 2nd carbon and a methylene group (CH2) at the 6th carbon. This molecule is part of the alkene class and exhibits the typical properties of alkenes, such as reactivity with electrophiles and the ability to undergo addition reactions. It is used in the synthesis of various organic compounds and can be found in the chemical industry for the production of polymers and other specialty chemicals.

1686-30-2

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1686-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1686-30-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1686-30:
(6*1)+(5*6)+(4*8)+(3*6)+(2*3)+(1*0)=92
92 % 10 = 2
So 1686-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16/c1-5-10(4)8-6-7-9(2)3/h5H,1-2,4,6-8H2,3H3

1686-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-6-methylideneocta-1,7-diene

1.2 Other means of identification

Product number -
Other names 2-Methyl-6-methylene-1,7-octadiene

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:1686-30-2 SDS

1686-30-2Downstream Products

1686-30-2Relevant academic research and scientific papers

7-METHYL-3-METHYLENE-7-OCTENYL HALIDE, METHOD FOR PRODUCING THE SAME, AND METHOD FOR PRODUCING 7-METHYL-3-METHYLENE-7-OCTENYL PROPIONATE

-

, (2016/07/27)

Provided is a simple, selective and efficient method for producing 7-methyl-3-methylene-7-octenyl propionate and the like. More specifically, provided is, for example, a method for producing 7-methyl-3-methylene-7-octenyl propionate, comprising the steps of: subjecting a nucleophile represented by Formula (1) and an electrophile represented by Formula (2) to a coupling reaction to obtain a 7-methyl-3-methylene-7-octenyl halide represented by Formula (3), and subjecting the 7-methyl-3-methylene-7-octenyl halide (3) to propionyloxylation to obtain the 7-methyl-3-methylene-7-octenyl propionate represented by Formula (4).

Monoterpenoid Synthesis by Transition Metal Catalyzed Coupling of Enediylmagnesium with C5-Organic Halides

Kajihara, Yasushi,Ishikawa, Katsuhiro,Yasuda, Hajime,Nakamura, Akira

, p. 3035 - 3036 (2007/10/02)

A series of isoprene coupling dimers bonded at 1-2, 1-3, 1-4, 2-4, 3-4, or 4-4 position was prepared by regiocontrolled catalysis of transition metals or without catalysts in the reaction of 2-methyl-2-butene-1,4-diylmagnesium or 3-methyl-2-butenylmagnesium chloride with C5-alkenyl halides.

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