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Imidazo[4,5-d]imidazole, octahydro-1,3,4,6-tetrakis(phenylmethyl)-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144437-22-9

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144437-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144437-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,3 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144437-22:
(8*1)+(7*4)+(6*4)+(5*4)+(4*3)+(3*7)+(2*2)+(1*2)=119
119 % 10 = 9
So 144437-22-9 is a valid CAS Registry Number.

144437-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,4,6-tetrabenzyl-2,3a,5,6a-tetrahydroimidazo[4,5-d]imidazole

1.2 Other means of identification

Product number -
Other names -

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:144437-22-9 SDS

144437-22-9Relevant academic research and scientific papers

Double Ci-H bond activation of C(sp3)H2 groups for the preparation of complexes with back-to-back bisimidazolinylidenes

Prades, Amparo,Poyatos, MacArena,Mata, Jose A.,Peris, Eduardo

scheme or table, p. 7666 - 7669 (2011/10/05)

Two-headed carbenes: N-heterocyclic carbene complexes of rhodium and iridium were obtained by the double Ci-H activation of CH2 groups in N heterocycles (see structure: C gray, N blue, Cl green, Ir pink). The reaction constitutes a valuable approach to new carbene ligands with unprecedented architectures. Copyright

Polyazapolycyclics by Condensation of Aldehydes with Amines. 3. Formation of 2,4,6,8-Tetrabenzyl-2,4,6,8-tetraazabicyclooctanes from Formaldehyde, Glyoxal, and Benzylamines

Nielsen, Arnold T.,Nissan, Robin A.,Chafin, Andrew P.,Gilardi, Richard D.,George, Clifford F.

, p. 6756 - 6759 (2007/10/02)

The condensation of formaldehyde, glyoxal, and benzylamine, in a stoichiometric ratio, leads to 2,4,6,8-tetrabenzyl-2,4,6,8-tetraazabicyclooctane (1d) in methanol solvent with formic acid catalyst.Six phenyl-sbstituted derivatives of 1d, as well as

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