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1,2,4-Trioxolane, 3,5-diphenyl-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21072-45-7

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21072-45-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21072-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,7 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21072-45:
(7*2)+(6*1)+(5*0)+(4*7)+(3*2)+(2*4)+(1*5)=67
67 % 10 = 7
So 21072-45-7 is a valid CAS Registry Number.

21072-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-3,5-diphenyl-1,2,4-trioxolane

1.2 Other means of identification

Product number -
Other names cis-stilbene ozonide

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:21072-45-7 SDS

21072-45-7Downstream Products

21072-45-7Relevant academic research and scientific papers

Ozonolysis of Vinyl Ethers in Solution and on Polyethylene

Griesbaum, Karl,Kim, Woo-Sun,Nakamura, Norinaga,Mori, Mitsuyuki,Nojima, Masatomo,Shigekazu, Kusabayashi

, p. 6153 - 6161 (2007/10/02)

Ozonolyses of the vinyl ethers 1a-f in methanol afforded almost exclusively the corresponding α-methoxy hydroperoxides 4, suggesting the preferred formation of the carbonyl oxides 2.In aprotic solvents including methyl formate, the predominant modes of decay of the carbonyl oxides 2 were cyclodimerization, reduction, and rearrangement, yet no ozonide formation.By contrast, ozonolyses of 1a-f on polyethylene gave the α-methoxy-substituted ozonides 14 in fair yields.Ozonolyzes of 1a-f in the presence of added carbonyl compounds 6 in methylene chloride or ether yielded the corresponding cross ozonides.Judged from the ozonide yields, the reactivities of the carbonyl compounds follow the sequence: (ClCH2)2C=O > ClCH2COCH3 > (CH3)2C=O and 2-CF3C6H4CHO > PhCHO.

Simultaneous Capture of Two Distinct Radical Ion Intermediates Generated from the EDA Complexes of Three-Membered Compounds with TCNE by Photoexcitation and in the Dark

Miyashi, Tsutomu,Kamata, Masaki,Mukai, Toshio

, p. 2780 - 2788 (2007/10/02)

Irradiation of the electron donor-acceptor (EDA) complexes of 2,2-diaryl-1-methylenecyclopropanes, 1,1,2,2-tetraarylcyclopropanes, 2,3-diaryloxiranes, or 2,3-diarylaziridines with tetracyanoethylene (TCNE) under aerated conditions involved oxygenation and

Stereoselective Oxygenation of 2,3-Diaryloxiranes by Irradiation of Electron Donor-Acceptor Complexes of Tetracyanoethylene

Miyashi, Tsutomu,Kamata, Masaki,Mukai, Toshio

, p. 1577 - 1579 (2007/10/02)

On irradiation of the electron donor-acceptor complexes of 2,3-diaryloxiranes with tetracyanoethylene (TCNE) in the presence of oxygen, cis-trioxolanes are formed stereoselectively; a nonstereoselective cycloaddition with TCNE competes with trioxol

THE PHOTOCHEMICAL PREPARATION OF OZONIDES BY ELECTRON-TRANSFER PHOTO-OXYGENATION OF EPOXIDES

Schaap, A. Paul,Siddiqui, Shahabuddin,Prasad, Girija,Palomino, Eduardo,Sandison, Mark

, p. 2229 - 2236 (2007/10/02)

9,10-Dicyanoanthracene (DCA) sensitizes the electron-transfer photo-oxygenation of epoxides in oxygen-saturated acetonitrile to form ozonides.Epoxides with oxidation potentials lower than 2 V vs SCE quench the fluorescence of DCA and are converted to the

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