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

15592-50-4

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15592-50-4 Usage

Type of compound

Cyclic organic peroxide

Common uses

a. Reagent in organic synthesis
b. Precursor to other chemicals

Stability

Highly reactive and unstable

Decomposition

Releases oxygen and heat upon decomposition

Safety precautions

Requires careful handling and storage

Pharmaceutical research

Potential anti-cancer agent and in the development of new drugs

Industrial and research applications

Versatile reactivity and potential biological activity

Check Digit Verification of cas no

The CAS Registry Mumber 15592-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,9 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15592-50:
(7*1)+(6*5)+(5*5)+(4*9)+(3*2)+(2*5)+(1*0)=114
114 % 10 = 4
So 15592-50-4 is a valid CAS Registry Number.

15592-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,5,5-tetramethyl-1,2,4-trioxolane

1.2 Other means of identification

Product number -
Other names 1,2,4-Trioxolane,3,3,5,5-tetramethyl

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:15592-50-4 SDS

15592-50-4Downstream Products

15592-50-4Relevant academic research and scientific papers

Ozonolyses of O-alkylated ketoximes in the presence of carbonyl groups: A facile access to ozonides

Griesbaum, Karl,Liu, Xuejun,Kassiaris, Athanassios,Scherer, Martin

, p. 1381 - 1390 (1997)

Ozonolyses of O-methyl oximes of acyclic ketones (7, 10, 19) and of cyclic ketones (16, 24, 27, 31) in the presence of acyclic ketones (8, 9, 17) or of cyclic ketones (18, 25, 26, 31) gave the corresponding tetrasubstituted cross-ozonides (13, 21, 29, 32). Ozonolyses of O-methylated monooximes of 1,4-, 1,5-, and 1,6-dicarbonyl compounds (35b-f) gave the corresponding bicyclic ozonides 36b-f. VCH Verlagsgesellschaft mbH, 1997.

Ozonolysis of Tetrasubstituted Ethylenes, Cycloolefins, and Conjugated Dienes on Polyethylene

Griesbaum, Karl,Volpp, Willi,Greinert, Reinhard,Greunig, Hans-Joachim,Schmid, Jurgen,Henke, Henning

, p. 383 - 389 (2007/10/02)

Ozonolyses of four tetrasubstituted ethylenes (7a-d), of two medium-sized cycloolefins (10a,b), and of norbornene (14) on polyethylene gave the corresponding ozonides, which could not be obtained by ozonolyses in solution.Ozonolyses of three conjugated dienes (25a,b,28) on polyethylene gave the corresponding diozonides, as the first examples of this class of ozonides.The thermal decomposition of some of the ozonides has been studied.

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