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24578-06-1

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  • 3,4-Pyrrolidinediol,2-[(1S)-1,2-dihydroxyethyl]-, (2R,3S,4S)-

    Cas No: 24578-06-1

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24578-06-1 Usage

General Description

The chemical (2R,3S,4S)-2-[(1R)-1,2-dihydroxyethyl]pyrrolidine-3,4-diol, also known as L-threo-1-phenyl-2-palmitoylamino-3-morpholinopropan-1-ol, is a compound with a pyrrolidine structure and two hydroxyl groups. It is a chiral molecule with multiple stereocenters, consisting of two asymmetric carbon atoms. (2R,3S,4S)-2-[(1R)-1,2-dihydroxyethyl]pyrrolidine-3,4-diol is commonly used as a building block in the synthesis of various pharmaceuticals and chiral ligands for asymmetric catalysis. It has also been studied for its potential therapeutic properties, particularly in the treatment of cardiovascular related diseases. Due to its stereochemistry and functional groups, this compound has shown to have high potential in medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 24578-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,7 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24578-06:
(7*2)+(6*4)+(5*5)+(4*7)+(3*8)+(2*0)+(1*6)=121
121 % 10 = 1
So 24578-06-1 is a valid CAS Registry Number.

24578-06-1SDS

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 (2R,3S,4S)-2-[(1R)-1,2-dihydroxyethyl]pyrrolidine-3,4-diol

1.2 Other means of identification

Product number -
Other names 1,4-Dideoxy-1,4-imino-D-glucitol

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:24578-06-1 SDS

24578-06-1Downstream Products

24578-06-1Relevant articles and documents

Synthesis and investigation of polyhydroxylated pyrrolidine derivatives as novel chemotypes showing dual activity as glucosidase and aldose reductase inhibitors

Guazzelli, Lorenzo,D'Andrea, Felicia,Sartini, Stefania,Giorgelli, Francesco,Confini, Gianluca,Quattrini, Luca,Piano, Ilaria,Nencetti, Susanna,Orlandini, Elisabetta,Gargini, Claudia,La Motta, Concettina

supporting information, (2019/09/30)

Diabetes is a multi-factorial disorder that should be treated with multi-effective compounds. Here we describe the access to polyhydroxylated pyrrolidines, belonging to the D-gluco and D-galacto series, through aminocyclization reactions of two differenti

A SHORT, VERSATILE APPROACH TO POLYHYDROXYLATED PYRROLIDINES UTILIZING A REDUCTIVE ELIMINATION-REDUCTIVE AMINATION AS A KEY STEP

Bernotas, Ronald C.

, p. 469 - 472 (2007/10/02)

An efficient synthesis of epimeric alpha-vinyl pyrrolidines starting from methyl 4,6-O-benzyliden gluco- and galactopyranosides gave ready access to hydroxylated pyrrolidines.

SYNTHESIS OF 1,4-DIDEOXY-1,4-IMINO-D-GLUCITOL, A GLUCOSIDASE INHIBITOR

Kuszmann, Janos,Kiss, Laszlo

, p. 45 - 54 (2007/10/02)

1,2:5,6-Di-O-isopropylidene-D-glucitol was converted via its 1,4-dimethanesulfonate into the 1-azido-4-methanesulfonate which, after deprotection and treatment with barium hydroxide, afforded a 9:1 mixture of the corresponding 3,4- and 4,5-anhydro derivat

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