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107657-57-8

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107657-57-8 Usage

Description

(3S)-3-(1-oxo-1,3-dihydro-2H-isoindol-2-yl)piperidine-2,6-dione is a complex chemical compound that belongs to the class of piperidine-2,6-dione compounds. It features an isoindol-2-yl group and the "(3S)" in its name denotes the stereochemistry of the molecule, which is crucial for its properties and potential applications. This unique structure and the presence of functional groups suggest that it may have a range of uses in various fields.

Uses

Used in Pharmaceutical Industry:
(3S)-3-(1-oxo-1,3-dihydro-2H-isoindol-2-yl)piperidine-2,6-dione is used as a potential pharmaceutical compound for its unique molecular structure and functional groups. It may contribute to the development of new drugs due to its specific stereochemistry and the presence of the isoindol-2-yl group, which can be key in designing molecules with targeted therapeutic effects.
Used in Organic Synthesis:
In the field of organic synthesis, (3S)-3-(1-oxo-1,3-dihydro-2H-isoindol-2-yl)piperidine-2,6-dione serves as a valuable intermediate or building block. Its complex structure allows for further chemical modifications, enabling the synthesis of a variety of organic compounds with diverse applications.
Used as a Reagent in Chemical Reactions:
(3S)-3-(1-oxo-1,3-dihydro-2H-isoindol-2-yl)piperidine-2,6-dione can be utilized as a reagent in various chemical reactions. Its functional groups and stereochemistry make it suitable for use in specific transformations, potentially leading to the formation of new compounds with unique properties.
Further research and studies are necessary to fully understand the properties and potential uses of (3S)-3-(1-oxo-1,3-dihydro-2H-isoindol-2-yl)piperidine-2,6-dione, as its complex structure and functional groups may unlock new possibilities in multiple industries.

Check Digit Verification of cas no

The CAS Registry Mumber 107657-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,6,5 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107657-57:
(8*1)+(7*0)+(6*7)+(5*6)+(4*5)+(3*7)+(2*5)+(1*7)=138
138 % 10 = 8
So 107657-57-8 is a valid CAS Registry Number.

107657-57-8SDS

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 (3S)-3-(3-oxo-1H-isoindol-2-yl)piperidine-2,6-dione

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 -
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More Details:107657-57-8 SDS

107657-57-8Downstream Products

107657-57-8Relevant articles and documents

COMPOUNDS MODULATING PROTEIN RECRUITMENT AND/OR DEGRADATION

-

Paragraph 0454; 0455; 0502; 0503, (2021/06/26)

The invention provides cereblon binders for the degradation of proteins by the ubiquitin proteasome pathway for therapeutic applications.

THALIDOMIDE ANALOGS AND METHODS OF USE

-

, (2017/08/01)

Thalidomide analogs and methods of using the thalidomide analogs are disclosed. Some embodiments of the disclosed compounds exhibit anti- angiogenic and/or anti-inflammatory activity. Certain embodiments of the disclosed compounds are non-teratogenic.

A facile scheme for phthalimide ? phthalimidine conversion

Luzzio, Frederick A.,Piatt Zacherl, DeAnna,Figg, William D.

, p. 2087 - 2090 (2007/10/03)

Desulfurization of phenylthiolactams using an ultrasound-promoted Raney nickel protocol yields the corresponding N-substituted phthalimidines. Benzylic oxidation of the N-substituted phthalimidines by treatment with 2,2'-bipyridinium chlorochromate/m-chloroperbenzoic acid (BPCC/MCPBA) affords the original phthalimides. The reduction-desulfurization is applied to the preparation of a deoxythalidomide derivative which is a TNF-α inhibitor.

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