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3412-49-5

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3412-49-5 Usage

General Description

(R)-4-phenyloxazolidine-2,5-dione, also known as (R)-POD, is a chemical compound with a cyclic structure containing an oxazolidine core. It is a chiral compound, meaning it has a specific three-dimensional arrangement of atoms that gives it mirror-image isomers. (R)-POD has been used in various chemical reactions and synthesis processes, particularly in the production of chiral building blocks for pharmaceuticals and agrochemicals. Its unique properties make it a valuable tool in asymmetric catalysis and other stereoselective transformations. Additionally, (R)-POD has demonstrated potential as a ligand in metal-catalyzed reactions and as a chiral auxiliary in asymmetric synthesis. Its versatility and reactivity make it a valuable molecule in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 3412-49-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3412-49:
(6*3)+(5*4)+(4*1)+(3*2)+(2*4)+(1*9)=65
65 % 10 = 5
So 3412-49-5 is a valid CAS Registry Number.

3412-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-4-PHENYLOXAZOLIDINE-2,5-DIONE

1.2 Other means of identification

Product number -
Other names N-carboxy-(R)-phenylglycine anhydride

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:3412-49-5 SDS

3412-49-5Relevant articles and documents

Footprint catalysis. IX. Molecular footprint catalytic cavities imprinted with chiral hydantoins; enantioselective hydantoinase mimics

Matsuishi,Shimada,Morihara

, p. 748 - 756 (2007/10/02)

Imprinting using chiral 5-phenyhydantoins ((5R)- and (5S)-5-pheny-2,4-imidazolinedione) as templates could mark chiral molecular footprint-like cavities on a silica (alumina) gel surface. These cavities displayed evident enantioselective catalyses in reac

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