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22824-83-5

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22824-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22824-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,2 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22824-83:
(7*2)+(6*2)+(5*8)+(4*2)+(3*4)+(2*8)+(1*3)=105
105 % 10 = 5
So 22824-83-5 is a valid CAS Registry Number.

22824-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2'-acetyl-9,9'-spirobi[fluorene]-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2.2'-Diacetyl-9-9'-spirobifluoren

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:22824-83-5 SDS

22824-83-5Relevant articles and documents

Efficient Rare-Earth-Based Coordination Polymers as Green Photocatalysts for the Synthesis of Imines at Room Temperature

Aguirre-Díaz, Lina M.,Snejko, Natalia,Iglesias, Marta,Sánchez, Félix,Gutiérrez-Puebla, Enrique,Monge, M. ángeles

, p. 6883 - 6892 (2018/06/26)

Five new rare-earth coordination polymers (CPs) were designed in order to offer a remarkable platform that contains light-harvesting antennas and catalytic active centers to achieve solar-energy conversion as green alternatives in the synthesis of imines. These five new spirobifluorene-containing Ln-CPs, named [Er3(Hsfdc)3(sfdc)3(H2O)]·xH2O (RPF-30-Er), [Ln(Hsfdc)(sfdc)(EtOH)]·S (RPF-31-Ln, where Ln = La, Nd, and Sm and S = H2O or EtOH), and [Ho(Hsfdc)(sfdc)(H2O)] (RPF-32-Ho) (RPF = rare-earth polymeric framework and H2sfdc = 9,9′-spirobi[9H-fluorene]-2,2′-dicarboxylic acid), have been solvothermally synthesized, and their structural features can be described as follows: (i) RPF-30-Er shows a 3D framework in which the inorganic trimers (secondary building units) are cross-linked by Hsfdc- and sfdc2- linkers displaying a pcu topology. (ii) The isostructural RPF-31-Ln series of materials, together with RPF-32-Ho, exhibit a 1D network of chains growing along the a axis with a ribbon-of-rings topology type. The photocatalytic activity of the RPF-n materials was tested in the oxidative coupling of amines using molecular oxygen and air as oxidizing agents under warm light. Among the materials investigated, RPF-31-Nd was chosen to further investigate the approach in the selectivity of different amine derivates.

O-HYDROXY-FUNCTIONALIZED DIAMINES, POLYMIDES, METHODS OF MAKING EACH, AND METHODS OF USE

-

Page/Page column 15, (2016/02/05)

Embodiments of the present disclosure provide for an ortho (o)-hydroxy-functionalized diamine, a method of making an o-hydroxy-functionalized diamine, an o-hydroxy-functionalized diamine-based polyimide, a method of making an o-hydroxy-functionalized diamine imide, methods of gas separation, and the like.

Synthesis, Chiral Resolution, and Absolute Configuration of C 2-Symmetric, Chiral 9,9′-Spirobifluorenes

Stobe, Caroline,Seto, Ryota,Schneider, Andreas,Lützen, Arne

, p. 6513 - 6518 (2016/02/18)

Racemic 2,2′-, 2,2′,7,7′-, and 2,2′,3,3′-substituted 9,9′-spirobifluorenes were synthesised and successfully resolved by HPLC on a Chiralpak IA stationary phase on both analytical and semipreparative scales. Their absolute configurations were determined by comparison of their specific optical rotations with literature data or by comparison of retention times with independently prepared enantiopure material. These compounds are versatile C 2-symmetric building blocks for the formation of more sophisticated cleft-like, chiral molecular architectures. Dissymmetric difunctionalised 9,9′-spirobifluorene derivatives were prepared and resolved by HPLC on a chiral stationary phase on a semipreparative scale. The absolute configurations of the resolved enantiomers were assigned by comparison of specific optical rotations with literature data or retention times of independently prepared enantiomerically pure material.

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