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245728-73-8

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245728-73-8 Usage

General Description

2-[(1R)-3-HYDROXY-1-METHYLPROPYL]-1H-ISOINDOLE-1,3(2H)-DIONE is a chemical compound with the molecular formula C12H13NO3. It is a type of isoindole-1,3(2H)-dione derivative, which is a class of compounds that are used in the synthesis of pharmaceuticals and are known for their potential pharmacological properties. This specific compound contains a hydroxyl group and a methyl group attached to a chiral carbon, giving it stereochemical properties. It may have various potential uses in the pharmaceutical industry, such as in drug development or as a research tool in biological studies. Further research is needed to determine its specific potential applications and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 245728-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,7,2 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 245728-73:
(8*2)+(7*4)+(6*5)+(5*7)+(4*2)+(3*8)+(2*7)+(1*3)=158
158 % 10 = 8
So 245728-73-8 is a valid CAS Registry Number.

245728-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(1R)-3-HYDROXY-1-METHYLPROPYL]-1H-ISOINDOLE-1,3(2H)-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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:245728-73-8 SDS

245728-73-8Relevant articles and documents

Stereoselective chemoenzymatic synthesis of both enantiomers of protected 4-amino-2-pentanone

Besse, Pascale,Ciblat, Stephane,Canet, Jean-Louis,Troin, Yves,Veschambre, Henri

, p. 2213 - 2224 (1999)

An acetal protected 4-amino-2-pentanone was synthesised by two different routes in 10 and seven steps, respectively, the key step being a microbiological reduction. Both enantiomers of the amine were obtained enantiomerically pure.

Synthesis and in vitro sodium channel blocking activity evaluation of novel homochiral mexiletine analogs

Carocci, Alessia,Catalano, Alessia,Bruno, Claudio,Lentini, Giovanni,Franchini, Carlo,De Bellis, Michela,De Luca, Annamaria,Camerino, Diana Conte

scheme or table, p. 299 - 307 (2010/10/21)

New chiral mexiletine analogs were synthesized in their optically active forms and evaluated in vitro as use-dependent blockers of skeletal muscle sodium channels. Tests carried out on sodium currents of single muscle fibers of Rana esculenta demonstrated

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