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4H-1,3,4,5-Oxatriazine, 4-(4-bromophenyl)-2,6-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112342-40-2

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112342-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112342-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,3,4 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112342-40:
(8*1)+(7*1)+(6*2)+(5*3)+(4*4)+(3*2)+(2*4)+(1*0)=72
72 % 10 = 2
So 112342-40-2 is a valid CAS Registry Number.

112342-40-2SDS

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 4-(4-bromophenyl)-2,6-diphenyl-1,3,4,5-oxatriazine

1.2 Other means of identification

Product number -
Other names 4-(p-Bromophenyl)-2,6-diphenyl-4H-1,3,4,5-oxatriazine

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:112342-40-2 SDS

112342-40-2Downstream Products

112342-40-2Relevant academic research and scientific papers

Substituted Bicyclic and Tricyclic Oxazolo-1,2,3-Triazole Systems: Ring Expansions to 1,3,4,5-Oxatriazines and Ring Contractions to 1,2,3-Triazaspiroalkane Derivatives

Butler, Richard N.,O'Shea, Donal F.

, p. 2797 - 2800 (2007/10/02)

Synthesis of a range of new bicyclic and tricyclic fused oxazolo-1,2,3-triazole systems is described.Treatment of these with acid caused transformations to substituted 1,3,4,5-oxatriazine and new 1,2,3-triazaspiroalkane systems which were isolated in high yields.Kinetic studies of the ring transformations indicated the presence of a delocalised carbocation intermediate and the mechanism of the ring expansion and contraction is discussed.

8?-Six-Atom Rings: 1,3,4,5-Oxa- and -Thia-triazines and 1,2,3,5-Tetrazines from an Extended Tandem Reaction: Reactions of 1,2,3-Triazolium-1-imides with (E)-Cinnamaldehyde, Methyl Cyanodithioformate, and Aryl-N-sulphinylamines: New Tetrahydro-oxazolo<4,5-

Butler, Richard N.,Evans, Ann M.,McNeela, Eithne M.,O'Halloran, Gerard A.,O'Shea, Paul D.,et al.

, p. 2527 - 2536 (2007/10/02)

The reactions of substituted 1,2,3-triazolium-1-imides with (E)-cinnamaldehyde, methyl cyanodithioformate, and aryl-N-sulphinylamines gave rise to substituted 1,3,4,5-oxatriazines, 1,3,4,5-thiatriazines, and 1,2,3,5-tetrazines, respectively.Each of these

Substituted 1,3,3a,4,5,6a-Hexahydro-oxazolo-1,2,3-triazoles from a Cycloaddition on a Carbonyl Group. Thermal Ring Expansion: A New Route to Substituted 1,3,4,5-Oxatriazenes

Butler, Richard N.,Evans, Ann M.,McArdle, Patrick,Cunningham, D.

, p. 1090 - 1091 (2007/10/02)

Substituted derivatives of hexahydro-oxazolo-1,2,3-triazoles, a new ring system, are described, and the crystal structure of one derivative is reported; on being heated they undergo a ring expansion providing a simple new route to the rare 1,3,4,5-

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