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90027-02-4

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90027-02-4 Usage

Structure

Bicyclic, containing a triazine ring and an azabenzene ring

Ligands

Can bind to metal catalysts, particularly palladium and platinum

Use in organic synthesis

Selective hydrogenation of unsaturated compounds

Affinity for metals

High affinity for metals such as palladium and platinum

Potential applications

Organic light-emitting diodes (OLEDs), chiral auxiliary in asymmetric synthesis, and various chemical and materials science applications.

Check Digit Verification of cas no

The CAS Registry Mumber 90027-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,2 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90027-02:
(7*9)+(6*0)+(5*0)+(4*2)+(3*7)+(2*0)+(1*2)=94
94 % 10 = 4
So 90027-02-4 is a valid CAS Registry Number.

90027-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-trimethyl-1,3,5-triazabicyclo[3.1.0]hexane

1.2 Other means of identification

Product number -
Other names 3.5.3'-Trimethyl-diaziridino <1'.2':1.2>1.2.4-triazolidin

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:90027-02-4 SDS

90027-02-4Relevant articles and documents

STEREOSPECIFITY OF 3JCH SPIN-SPIN COUPLING CONSTANTS IN BICYCLIC cis-DIAZIRINES: STEREOCHEMISTRY OF 2,4,6-TRIALKYL-1,3,5-TRIAZABICYCLOHEXANES

Denisenko, S. N.,Shustov, G. V.,Chervin, I. I.,Kostyanovskii, R. G.

, p. 1104 - 1109 (2007/10/02)

Stereospecifity of 3JC,N,C,H spin-spin coupling constants (3Jtrans > Jgauche) in the 13C NMR spectra of 1,5-diaza- and 1,3,5-triazabicyclohexanes was observed.Proceeding from this, the preferred conformations of the d,l and meso isomers of 2,4,6-trialkyl-1,3,5-triazabicyclohexanes were established, and a mechanism for the interconversion of these isomers via openings of the five-membered ring ans imino-enamine equilibrium was proposed.It is also shown, that the stereochemical result of the Schmitz reaction is determined in the step involving cyclization of the iminium intermediate.

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