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767-09-9

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767-09-9 Usage

General Description

1,2,4-Trioxolane, 3-butyl- is a chemical compound with the molecular formula C7H14O3. It is a type of trioxolane, which is a heterocyclic organic compound containing three oxygen atoms in a six-membered ring. 1,2,4-Trioxolane, 3-butyl- has a butyl group attached to the trioxolane ring, which imparts specific chemical and physical properties to the compound. This chemical is commonly used in organic synthesis and pharmaceutical research, and it may have potential applications in the development of new drugs or other biologically active compounds. Additionally, it is important to handle this chemical with caution, as it may pose hazards to human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 767-09-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 767-09:
(5*7)+(4*6)+(3*7)+(2*0)+(1*9)=89
89 % 10 = 9
So 767-09-9 is a valid CAS Registry Number.

767-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butyl-1,2,4-trioxolane

1.2 Other means of identification

Product number -
Other names 1-Hexene, 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:767-09-9 SDS

767-09-9Upstream product

767-09-9Relevant articles and documents

Formation of secondary ozonides in the gas phase low-temperature ozonation of primary and secondary alkenes

Fajgar, Radek,Vitek, Josef,Haas, Yehuda,Pola, Josef

, p. 239 - 248 (2007/10/03)

The gas-phase ozonation of a series of alkenes RCH=CH2 (R = Et, Hex), trans-RHC=CHR (R = Me, Et, Pri) and Me2C=CMe2 at -40 to 20°C, and that of ethene H2C=CH2 at -120 to 0°C at 10-4 v/v concentrations in N2 at atmospheric pressure have been studied. Using complementary product analysis by means of GC-FTIR and GC-MS techniques, we present conclusive evidence for the formation of secondary alkene ozonides as high-yield products in all instances except Me2C=CMe2. It is shown that the stereoselectivity for the conversion of trans-RHC=CHR (R = Me, Et, Pri) to trans-secondary ozonides in the gas phase is similar to that observed earlier in solution, and that the yields of secondary ozonides from RHC=CH2, but not those from RHC=CHR, significantly decrease with increasing temperature.

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