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1,6-Heptadiene, 4-(2-propenyl)-, also known as 4-allyl-1,6-heptadiene, is an organic compound with the molecular formula C10H16. It is a colorless liquid with a strong, pungent odor. This chemical is a conjugated diene, which means it has two carbon-carbon double bonds separated by a single bond, and it is also an allyl compound, as it contains an allyl group (CH2=CHCH2-). 1,6-Heptadiene, 4-(2-propenyl)- is used as an intermediate in the synthesis of various organic compounds, particularly in the production of fragrances and pharmaceuticals. It is also used as a building block for the preparation of polymers and other specialty chemicals. Due to its reactivity, it is important to handle 1,6-Heptadiene, 4-(2-propenyl)- with care, following proper safety protocols.

2946-82-9

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2946-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2946-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2946-82:
(6*2)+(5*9)+(4*4)+(3*6)+(2*8)+(1*2)=109
109 % 10 = 9
So 2946-82-9 is a valid CAS Registry Number.

2946-82-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-allyl-hepta-1,6-diene

1.2 Other means of identification

Product number -
Other names Triallylmethan

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:2946-82-9 SDS

2946-82-9Downstream Products

2946-82-9Relevant academic research and scientific papers

A novel iron complex for cross-coupling reactions of multiple C-Cl bonds in polychlorinated solvents with grignard reagents

Gartia, Yashraj,Pulla, Sharon,Ramidi, Punnamchandar,Farris, Carolina Costa,Nima, Zeid,Jones, Darin E.,Biris, Alexandru S.,Ghosh, Anindya

, p. 1397 - 1404 (2013/01/15)

A novel iron(III) complex (2) of a pincer ligand [1, N2,N6-bis(2,6- diisopropylphenyl)pyridine-2,6-dicarboxamide] was developed and used for remediation of polychlorinated solvents via sp3-sp3 coupling of Grignard reagents with C-Cl bonds. The use of an iron catalyst for such coupling reactions is highly desirable due to its greener and more economical nature. Complex 2 was characterized using various spectroscopic techniques: electrospray ionization mass spectrometer (ESI-MS, m/z 575.1), cyclic voltammetry (E 1/2, 0.03 V and ΔE, 0.97 V), and ultraviolet visible (UV/Vis) spectroscopic techniques. The iron(III) complex showed efficient activation of multiple C-Cl bonds and catalyzing C-C coupling of polychlorinated alkyl halides, such as dichloromethane (CH2Cl2), chloroform (CHCl3), and carbon tetrachloride (CCl4), with various Grignard reagents under ambient reaction conditions. Complex 2 showed exceptional activity with reactions approaching near completion in about 5 min. With the required catalyst loading as low as 0.2 mol%, considerably high turnover numbers (TON = 483) and turnover frequency (TOF = 5,800 h-1) were obtained. None of the products detected during the reaction contained any chlorine, indicating an efficient dechlorination method while synthesizing products of synthetic and commercial interest. Interestingly, the catalyst was capable of replacing all chlorine atoms in each polychlorinated solvent under the investigations with high conversion. Springer Science+Business Media, LLC 2012.

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