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2-Tetrahydrofuryl hydroperoxide (C4H8O2) is an organic compound that consists of a tetrahydrofuran ring with a hydroperoxy group attached to the 2-position. It is a colorless liquid with a pungent odor and is soluble in water and organic solvents. This chemical is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Due to its high reactivity, it is essential to handle 2-tetrahydrofuryl hydroperoxide with caution, as it can decompose and release oxygen, posing potential hazards.

4676-82-8

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4676-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4676-82-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4676-82:
(6*4)+(5*6)+(4*7)+(3*6)+(2*8)+(1*2)=118
118 % 10 = 8
So 4676-82-8 is a valid CAS Registry Number.

4676-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroperoxyoxolane

1.2 Other means of identification

Product number -
Other names 2-tetrahydrofuryl 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:4676-82-8 SDS

4676-82-8Relevant academic research and scientific papers

Interaction between the peroxide adduct of binuclear iron(III) complex with (HPTP) anion and the sugar moiety of nucleosides

Nishino, Satoshi,Kunita, Mami,Kobayashi, Teruyuki,Matsushima, Hideaki,Tokii, Tadashi,Nishida, Yuzo

, p. 1272 - 1276 (1999)

We have in this study obtained the experimental evidence to suggest that the peroxide adduct of binuclear iron(III) complex with H(HPTP) directly reacts with the sugar moiety of the DNA chain, to cleave it; H(HPTP) denotes N,N,N′,N′-tetrakis(2-pyridylmeth

Heteroarylation of Ethers, Amides, and Alcohols with Light and O2

Bhakat, Manotosh,Biswas, Promita,Dey, Jayanta,Guin, Joyram

supporting information, p. 6886 - 6890 (2021/09/14)

An efficient protocol for the Cα-H heteroarylation of ethers, amides, and alcohols using air and light under mild conditions is described. The reaction is applicable to a wide spectrum of functional groups. The generation of C-radicals via photoinduced aerobic oxidation of ethers, amides, and alcohols is the key feature of the process. Control experiments suggest a radical pathway for the reaction.

Cleavage of a carbon-carbon triple bond via gold-catalyzed cascade cyclization/oxidative cleavage reactions of (2)-enynols with molecular oxygen

Liu, Yuanhong,Song, Feijie,Guo, Shenghai

, p. 11332 - 11333 (2007/10/03)

A highly efficient carbon-carbon triple bond cleavage reaction of (Z)-enynols was developed, which offered a new route to highly substituted butenolides. The methodology is realized by a tandem reaction using a single gold(I) catalyst, which could catalyze different reactions of cyclization/oxidative cleavage in the same vessel. Copyright

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