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5H-Pyrrolo[3,4-b]pyrazine-5,7(6H)-dione, 2,3-dichloro-6-[4-(1,1-dimethylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

656236-79-2

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656236-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 656236-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,6,2,3 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 656236-79:
(8*6)+(7*5)+(6*6)+(5*2)+(4*3)+(3*6)+(2*7)+(1*9)=182
182 % 10 = 2
So 656236-79-2 is a valid CAS Registry Number.

656236-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dichloropyrazine-2,3-dicarboxylic acid 4-(tert-butyl)phenylimide

1.2 Other means of identification

Product number -
Other names 6-(4-tert-Butyl-phenyl)-2,3-dichloro-pyrrolo[3,4-b]pyrazine-5,7-dione

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:656236-79-2 SDS

656236-79-2Downstream Products

656236-79-2Relevant academic research and scientific papers

Functionalized and Partially or Differentially Bridged Resorcin[4]arene Cavitands: Synthesis and Solid-State Structures

Azov, Vladimir A.,Skinner, Philip J.,Yamakoshi, Yoko,Seiler, Paul,Gramlich, Volker,Diederich, Francois

, p. 3648 - 3670 (2003)

We report the synthesis and structural characterization of modified Cram-type, resorcin[4]arene-based cavitands. Two main loci on the cavitand backbone were selected for structural modification: the upper part (wall domain) and the lower part (legs). Synthesis of unsymmetrically bridged cavitands with different wall components (i.e., 7, 8, and 14-18) was performed by stepwise bridging of the four couples of neighboring, H-bonded OH-groups of octol la (Schemes 1, 2, 4, and 5). Cavitands with modified legs (i.e., 20, 24, 27, and 28), targeted for surface immobilization, were synthesized by short routes starting from suitable aldehyde starting materials incorporating either the fully preformed leg moieties or functional precursors to the final legs (Schemes 7-10). The new cavitand substitution patterns described in this paper should enable the construction of a wide variety of functional architectures in the future. X-Ray crystallography afforded the characterization of cavitands 2c (Fig. 3) and 24 (Fig. 7) in the vase conformation, with 2c featuring a well-ordered CH2Cl2 guest molecule in its cavity. A particular highlight is the X-ray crystal-structure determination of octanitro derivative 19 (Scheme 6), which, for the first time, shows a cavitand, lacking substituents in the ortho-position to the two O-atoms of the four resorcinol moieties, in the kite-conformation (Fig. 5).

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