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1-Hydroperoxyl-1-vinylcyclohexene-3, a cyclic organic peroxide, is a highly reactive and unstable chemical compound with a molecular formula of C8H12O2. Its structure features a vinyl group and a cyclohexene ring, making it susceptible to a range of chemical reactions such as polymerization and oxidation. Due to its high reactivity and potential for explosive decomposition, it requires careful handling.

3736-26-3

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3736-26-3 Usage

Uses

Used in Chemical Synthesis Industry:
1-Hydroperoxyl-1-vinylcyclohexene-3 is used as an intermediate in chemical synthesis for the production of various organic compounds and polymers. Its unique structure and reactivity make it a valuable component in the synthesis of a wide range of products.
Due to the lack of specific application reasons in the provided materials, the uses are generalized based on the compound's properties and typical applications in the chemical synthesis industry. If more detailed information about specific applications or industries is available, it can be incorporated into the response.

Check Digit Verification of cas no

The CAS Registry Mumber 3736-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3736-26:
(6*3)+(5*7)+(4*3)+(3*6)+(2*2)+(1*6)=93
93 % 10 = 3
So 3736-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-2-8(10-9)6-4-3-5-7-8/h2-4,9H,1,5-7H2

3736-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethenyl-4-hydroperoxycyclohexene

1.2 Other means of identification

Product number -
Other names Butadiene dimer hydroperoxide

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:3736-26-3 SDS

3736-26-3Upstream product

3736-26-3Downstream Products

3736-26-3Relevant academic research and scientific papers

Autoxidation of Vinylcyclopentane, Vinylcyclohexane, and 4-Vinylcyclohex-1-ene

Biela, R.,Bilas, W.,Ihsan, U.,Pritzkow, W.,Schmidt-Renner, W.

, p. 893 - 900 (2007/10/02)

The title olefins were oxidized with molecular oxygen at 75-80 deg C.About 40percent of the oxygen absorbed were found by iodometric titration as peroxidic oxygen.The reaction products were analyzed by a combination of chemical methods, gas chromatography, and 13C-n.m.r.-spectroscopy.Vinylcyclopentane and vinylcyclohexane are attacked preferably at the tertiary allylic C-H-bonds giving almost equimolar mixtures of the corresponding allylisomeric hydroperoxides.In the case of 4-vinylcyclohex-1-ene the C-H-bonds in position 6 are preferably attacked, but products of attack on the other allylic C-H-bonds also could be identified.In all cases the amount of products which could not be detected gaschromatographically was determined by balance experiments in the presence of an internal standard.

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