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3,6-epoxy- is a chemical prefix indicating the presence of an epoxy group at the 3 and 6 positions of a molecule. Epoxy compounds are characterized by the presence of an oxygen atom connected to two carbon atoms, forming a three-membered ring structure. These compounds are widely used in various industries, such as coatings, adhesives, and composite materials, due to their excellent adhesion, chemical resistance, and mechanical properties. The 3,6-epoxy- prefix specifically refers to the position of the epoxy group within the molecule, which can significantly influence the compound's reactivity and properties.

4378-84-1

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4378-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4378-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4378-84:
(6*4)+(5*3)+(4*7)+(3*8)+(2*8)+(1*4)=111
111 % 10 = 1
So 4378-84-1 is a valid CAS Registry Number.

4378-84-1SDS

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 12-oxahexacyclo[5.4.1.02,6.03,10.05,9.08,11]dodecane

1.2 Other means of identification

Product number -
Other names 8,11-oxopentacyclo[5.4.0.02,6.03,10.05,9]undecane

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:4378-84-1 SDS

4378-84-1Downstream Products

4378-84-1Relevant academic research and scientific papers

Efficient synthesis of 4-halo-D3-trishomocubane derivatives

Levandovskiy, Igor A.,Gaidai, Alexandr V.,Zhyhadlo, Yevheniia Y.,Sharapa, Dmitry I.,Shishkin, Oleg V.,Shishkina, Svitlana V.,Rassukana, Yuliya V.

, p. 373 - 383 (2019/01/03)

Reaction of Cs-trishomocubane-8,11-diol with hydrohalic acids results in haloalcohols – 4,7-disubstituted derivatives of D3-trishomocubane. The reaction involves the rearrangement of the trishomocubane skeleton and the stereoselective formation of 4,7-D3-trishomocubanediol and 5‐oxahexacyclo[5.4.1.02,6.03,10.04,8.09,12]-dodecane as side products. The mechanism of the rearrangement was proposed. 7-Halo-D3-trishomocuban-4-ols were oxidized to the corresponding haloketones. The structure of the major isomers of the haloketones was confirmed through X-ray analysis.

A NOVEL, VERSATILE SYNTHETIC APPROACH TO LINEARLY FUSED TRICYCLOPENTANOIDS via PHOTO-THERMAL OLEFIN METATHESIS

Mehta, Goverdhan,Srikrishna, A.,Reddy, A. Veera,Nair, Mangalam S.

, p. 4543 - 4559 (2007/10/02)

Fifteen examples of a new, speedy and general approach to linearly fused tricyclopentanoids bearing the tricyclo2,6>undecane (triquinane) frame of high contemporary interest is delineated.The key concept in our synthetic sequence to tri

The reaction of potassium iodide in polyhydrogen fluoride-pyridine with two cage diols. A simple synthesis of tetracyclo4,11.05,9>undeca-2,6-diene ('homohypostrophene')

Dong, Dao Cong,Edward, John T.

, p. 1324 - 1326 (2007/10/02)

The diol 2 was converted by treatment with potassium iodide in polyhydrogen fluoride-pyridine into a mixture of the diiodide 5 and homohypostrophene 6.The diol 10 under the same conditions gave the ether 14.Treatment of the mixture of 5 and 6 with sodium in boiling tetrahydrofuran gave an easily-separable mixture of 6 and 7.

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