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(E)-1-[2-(3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-en-5-yl)ethyl]-2-(2-phenylethyl)diazene is a complex organic compound characterized by its diazene functional group. It features a dioxatricyclo[5.1.0.0~2,4~]oct-5-en-5-yl)ethyl group and a 2-phenylethyl group attached to the diazene center. (E)-1-[2-(3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-en-5-yl)ethyl]-2-(2-phenylethyl)diazene exhibits a trans configuration around the diazene double bond, as indicated by the (E) prefix. As a synthetically derived molecule, it may hold potential applications in various fields such as pharmaceuticals, materials science, and organic synthesis. The intricate structure and unique features of (E)-1-[2-(3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-en-5-yl)ethyl]-2-(2-phenylethyl)diazene suggest that it could possess intriguing chemical and physical properties, making it a subject of interest for further research and exploration in the realm of organic chemistry.

3378-37-8

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3378-37-8 Usage

Uses

Used in Pharmaceutical Applications:
(E)-1-[2-(3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-en-5-yl)ethyl]-2-(2-phenylethyl)diazene is used as a potential pharmaceutical agent for [application reason]. Its unique structural features and diazene functional group may contribute to its effectiveness in this application.
Used in Materials Science:
In the field of materials science, (E)-1-[2-(3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-en-5-yl)ethyl]-2-(2-phenylethyl)diazene is used as a component in the development of novel materials for [application reason]. Its complex structure and properties could be harnessed to create innovative materials with specific characteristics.
Used in Organic Synthesis:
(E)-1-[2-(3,8-dioxatricyclo[5.1.0.0~2,4~]oct-5-en-5-yl)ethyl]-2-(2-phenylethyl)diazene serves as a key intermediate in organic synthesis for the production of various complex organic molecules. Its unique structural features make it a valuable building block for the synthesis of other compounds with potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3378-37-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3378-37:
(6*3)+(5*3)+(4*7)+(3*8)+(2*3)+(1*7)=98
98 % 10 = 8
So 3378-37-8 is a valid CAS Registry Number.

3378-37-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Diazene, bis(2-phenylethyl)-, dioxide

1.2 Other means of identification

Product number -
Other names 4-hydroxy-3-nitroso-1-naphthalenesulfonicaci

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:3378-37-8 SDS

3378-37-8Upstream product

3378-37-8Relevant academic research and scientific papers

Direct transformation of benzilic amines to carbonyls using polyacrylamide-bound tungstate under phase-transfer catalysis conditions

Hamamoto, Hiromi,Suzuki, Yachiyo,Takahashi, Hideyo,Ikegami, Shiro

, p. 4239 - 4242 (2008/02/08)

A recyclable catalytic system under heterogeneous phase-transfer catalysis conditions was designed by using polyacrylamide-bound tungstate. A convenient method for the oxidative direct transformation of benzilic amines to carbonyls with hydrogen peroxide was then developed.

Methyltrioxorhenium-Catalyzed Oxidation of Secondary and Primary Amines with Hydrogen Peroxide

Yamazaki, Shigekazu

, p. 877 - 883 (2007/10/03)

The methyltrioxorhenium-catalyzed oxidation of secondary amines and primary amines with hydrogen peroxide has been carried out. The oxidation of secondary amines afforded nitrones in good-to-excellent yield. Benzylamines were selectively oxidized to oximes, while general primary alkylamines possessing the α-C -H bond gave mixtures of oximes, nitroso dimers, and azoxy compounds.

OXIDATION OF PRIMARY ALIPHATIC AMINES WITH SODIUM PERBORATE

Zajac, Walter W.,Darcy, Michael G.,Subong, Amador P.,Buzby, John H.

, p. 6495 - 6496 (2007/10/02)

A biphasic system of ethyl acetate and water containing sodium perborate, sodium bicarbonate and N,N,N',N'-tetraacetylethylenediamine oxidizes primary aliphatic amines to aliphatic C-nitroso compounds in good to excellent yields.

Oxidation of Primary Aliphatic Amines to C-Nitroso Dimers

Zajac, Walter W.,Walters, Thomas R.,Woods, James M.

, p. 808 - 810 (2007/10/02)

A biphasic system of ethyl acetate or dichloromethane and water containing sodium percarbonate (Na2CO3*3/2H2O2), sodium hydrogen carbonate and N,N,N',N'-tetraacetylethylenediamine oxidizes primary aliphatic amines to aliphatic C-nitroso dimers in most cases in good to excellent yields.

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